ВОзвращает список болезней. Можно фильтр/искать

search, age, gender, parent, symptoms, sort_name, sort_by, rand, branches
GET /disease/?format=api&ordering=-image&page=54
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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                    "lead": "Хронический запор (хроническая констипация) – симптомокомплекс, включающий в себя уменьшение частоты актов дефекации и выраженные затруднения в процессе испражнения, выявляющиеся на протяжении полугода или более. Является полиэтиологическим патологическим состоянием, рассматривается в современной проктологии, как важнейшая социальная и медицинская проблема. Специалисты считают, что хроническими запорами различной степени выраженности страдают 30-50% взрослых и 5-20% детей США и стран Европы. Точные статистические данные о частоте запоров в России отсутствуют, поскольку пациенты стесняются или не считают нужным обращаться к врачам и нередко занимаются самолечением. С возрастом вероятность развития хронического запора увеличивается.\r\n\r\nНеспециалисты нередко полагают, что запором является состояние, при котором акт дефекации осуществляется реже, чем 1 раз в сутки. Такой подход приводит к самостоятельной гипердиагностике и необоснованному приему слабительных препаратов. Между тем, физиологической нормой условно считается частота испражнений от 3 раз в день до 3 раз в неделю. Для хронического запора характерно не только увеличение временного интервала между испражнениями, но и уменьшение количества фекальных масс, повышенная плотность, сухость и твердость кала, а также ощущение неполного опорожнения кишечника после акта дефекации. При хроническом запоре могут наблюдаться как все перечисленные признаки, так и один или два из них, при этом выраженность того или иного признака может сильно различаться.",
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            },
            "code": "E68",
            "name": "Последствия избыточности питания",
            "icd_name": "Последствия избыточности питания",
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            "lead": "Ожирение",
            "description": " \r\n\r\nТермин ожирение алиментарно-конституционального генеза или первичное ожирение подразумевает расстройство в функционировании организма, спровоцированное нехваткой двигательной активности и неправильно составленным рационом питания – так называемым перееданием. \r\n",
            "etiology": "<p>Эндогенные (внутренние) причины развития болезни:  </p>\r\n<ul>\r\n<li>Генетическая предрасположенность – если в семье есть люди, страдающие от этого заболевания, то риск его развития у следующих поколений повышен; </li>\r\n<li>Строение жировой ткани, скорость обмена жиров; </li>\r\n<li>Активность функционирования центров голода и сытости в гипоталамусе; </li>\r\n<li>Изменения гормонального фона, которые могут быть вызваны периодом беременности, родов и лактации, климактерическим синдромом.  </li>\r\n</ul>\r\n<p>К экзогенным (внешним) факторам развития заболевания относятся:  </p>\r\n<ul>\r\n<li>Ожирение алиментарно-конституционального генеза может быть вызвано избыточным потреблением пищи в любом возрасте, включая детский; </li>\r\n<li>Рефлексы, привязанные ко времени и количеству еды, – некоторые люди в стрессовых ситуациях успокаиваются только во время принятия пищи, другие отдыхают после рабочего дня на диване перед телевизором с тарелкой, полной любимых, но не всегда полезных продуктов; </li>\r\n<li>Национальные традиции, исходя из которых люди усваивают определенный тип, а также рацион питания; </li>\r\n<li>Распространенный во всем мире малоактивный образ жизни, приводящий к гиподинамии.</li>\r\n</ul>",
            "pathogenesis": "<p>  Алиментарное ожирение базируется на стимуляции секреции инсулина в результате обильной еды, повышении активности центра голода и торможения центра сытости, находящихся в гипоталамусе.  </p>\r\n<p>В патогенезе ожирения нельзя не придавать значения эндокринным органам и прежде всего гипофизу, надпочечникам, островковому аппарату поджелудочной железы, щитовидной и половым железам. </p>\r\n<p>Повышение функциональной активности системы гипофиз - кора надпочечников и инсулярного аппарата поджелудочной железы способствует накоплению жира в жировых депо. Снижение соматотропной активности аденогипофиза, сопровождающееся ослаблением процессов мобилизации жира из депо и последующего его окисления в печени, также выступает в качестве патогенетического фактора. </p>\r\n<p>Пониженное образование адреналина - активного липолитического фактора - имеет существенное значение в понижении мобилизации жира и является одним из патогенетических факторов ожирения.  </p>",
            "diagnostics": "<p>Для диагностики ожирения в практической медицине наиболее часто используют индекс массы тела (ИМТ). Применяется также индекс Борнгардта, в отличие от ИМТ учитывающий телосложение человека. </p>\r\n<p>Показателем для определения избыточного веса является Индекс массы тела (ИМТ). </p>\r\n<p>ИМТ = масса тела/рост2 (кг/м2).. </p>\r\n<p>Нормальной массе тела соответствует ИМТ 18,5-24,5. ИМТ 25,0-29,9 говорит об избытке массы тела, а ИМТ более 30 указывает на наличие у пациента ожирения. </p>\r\n<p>Диагноз I степени ставится при ИМТ 30,0 – 34,9,  </p>\r\n<p>II степени – при ИМТ 35,0 – 39,9,  </p>\r\n<p>III степени при ИМТ более 40.  </p>\r\n<p>Нужно помнить, что показатель ИМТ не является достоверным для детей, беременных, а также спортсменов и лиц с очень развитой мускулатурой. Для этих категорий пациентов наличие ожирения и его степень определяется по-другому. </p>\r\n<p>Наиболее точным методом определения количества жировой ткани в организме считается МРТ. </p>\r\n<p>В быту количество жировой ткани в организме человека обычно определяется бытовыми весами с анализатором состава тела методом биоимпедансометрии (метод диагностики состава тела человека посредством измерения импеданса – электрического сопротивления участков тела – в разных частях организма). </p>",
            "treatment": "<p>Основные способы лечения при избыточном весе и ожирении</p>\r\n<p>К ним относят соблюдение диеты с повышенным содержанием клетчатки, витаминов и других биологически активных компонентов (злаки и цельнозерновые продукты, овощи, фрукты, орехи, зелень и др.) и ограничением употребления легкоусваиваемых организмом углеводов (сахар, сладости, выпечка, хлебобулочные и макаронные изделия из муки высших сортов), а также физические упражнения. </p>\r\n<p>Общий подход при лекарственном лечении ожирения состоит в испытании всех известных препаратов для лечения ожирения.</p>\r\n<p>По механизму действия препараты для лечения ожирения делятся на три группы:  </p>\r\n<ol>\r\n<li>снижающие потребление пищи (подавляющие аппетит);  </li>\r\n<li>увеличивающие расход энергии;  </li>\r\n<li>уменьшающие всасывание питательных веществ. </li>\r\n</ol>\r\n<p>Если результат медикаментозного лечения оказывается незначительным или его нет, то необходимо прекратить такое лечение. Возможно рассмотрение вопроса целесообразности проведения хирургического лечения. Используют бариатрические операции (направленные на уменьшение объема желудка) и косметические операции (удаление излишков жировой ткани). </p>\r\n<p>Применяется также психотерапевтическое лечение (поведенческая терапия). </p>",
            "prevention": "<p>Людям со склонностью к избыточному весу следует уравновесить количество потребляемой пищи и уровень физических нагрузок. Диета должна быть сбалансированной. Увеличение физических нагрузок, занятия спортом должны идти вслед за изменением диеты.</p>",
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            "lead": "черепно-мозговая грыжа, содержащая оболочки и вещество головного мозга, но не включающая его желудочки",
            "description": "<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Энцефалоцеле &ndash; это порок развития черепа и головного мозга, при котором часть мозгового вещества оказывается вне черепной коробки вследствие дефекта костной ткани.</span></p>",
            "etiology": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Черепно-мозговые грыжи возникают вследствие неправильной закладки нервной трубки во внутриутробном развитии. Факторы, которые приводят к этому, четко не выявлены. Предполагается влияние вредных факторов на организм беременной женщины:</span></p>\r\n<ul style=\"margin-top: 0; margin-bottom: 0; padding-inline-start: 48px;\">\r\n<li style=\"list-style-type: disc; font-size: 6.5pt; font-family: Verdana; color: #333333; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre;\" dir=\"ltr\">\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">употребление наркотиков, алкоголя; курение;</span></p>\r\n</li>\r\n<li style=\"list-style-type: disc; font-size: 6.5pt; font-family: Verdana; color: #333333; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre;\" dir=\"ltr\">\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">злоупотребление лекарственными средствами;</span></p>\r\n</li>\r\n<li style=\"list-style-type: disc; font-size: 6.5pt; font-family: Verdana; color: #333333; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre;\" dir=\"ltr\">\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">частые простудные заболевания;</span></p>\r\n</li>\r\n<li style=\"list-style-type: disc; font-size: 6.5pt; font-family: Verdana; color: #333333; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre;\" dir=\"ltr\">\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">инфекционные болезни во время беременности: токсоплазмоз, краснуха;</span></p>\r\n</li>\r\n<li style=\"list-style-type: disc; font-size: 6.5pt; font-family: Verdana; color: #333333; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre;\" dir=\"ltr\">\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">внезапные нарушения эмбрионального развития.</span></p>\r\n</li>\r\n</ul>\r\n<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Также не стоит исключать и генетическую предрасположенность, ведь характерная аномалия, преобладающая у кровных родственников, часто распространяется и на будущее потомство.</span></p>",
            "pathogenesis": "",
            "diagnostics": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Первичная диагностика возможна уже в первые дни и часы жизни ребенка, поскольку образование визуализируется сразу после рождения. Любое опухолеподобное выпячивание изначально расценивается как энцефалоцеле с последующей дифференциальной диагностикой. Чаще всего приходится исключать полипы и ангиомы.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Диагноз уточняется на основании данных КТ и МРТ, при этом проводится серия снимков, подтверждающих наличие костного дефекта и присутствие мозговых тканей в выпячивании. Просвечивание (трансиллюминация) позволяет заподозрить наличие в образовании нервных тканей. Кроме того, даже легкое надавливание вызывает беспокойство пациента в связи с резким повышением внутричерепного давления.</span></p>",
            "treatment": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Лечение только оперативное. Срочность операции определяется состоянием ребенка. Чаще всего вмешательство по удалению энцефалоцеле планируется в возрасте от 3 лет. Такой срок необходим для того, чтобы понаблюдать за развитием головного мозга, в том числе за участком в составе выпячивания. Кроме того, ребенок этому времени уже достаточно окрепнет, чтобы благополучно перенести такую сложную операцию. Противопоказаниями являются повышенное внутричерепное давление, выраженные психические и неврологические расстройства. Истончение кожи над энцефалоцеле, наоборот, является показанием к срочному хирургическому вмешательству.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Операция осуществляется в два этапа. Сначала выполняется закрытие костного дефекта и отсечение ножки грыжи. В раннем возрасте отверстие в черепе можно закрыть лоскутом надкостницы, при более поздних операциях (в возрасте более 3 лет) применяется костный трансплантат.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Второй этап операции &ndash; косметическое иссечение поверхностно расположенной оставшейся части грыжевого мешка. Проводится через 15-20 дней после первого этапа (3-6 месяцев в случае интракраниального доступа). Тактику операции в каждом конкретном случае определяют в зависимости от степени вовлеченности мозговых тканей в энцефалоцеле.</span></p>",
            "prevention": "<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Врожденные деформации лица предупредить невозможно. Если в семье родился ребенок с подобной деформацией, то родителям желательно пройти медико-генетическое консультирование, чтобы иметь возможность оценить риск появления такой же аномалии у следующего ребенка.</span></p>",
            "clinical_picture": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Симптомы энцефалоцеле могут варьироваться от одного человека к другому в зависимости от многих различных факторов, включая размер, местоположение, количество и вид мозговой ткани, выступающей из черепа. Энцефалоцеле &mdash; врожденный порок развития, т.е. присутствующий при рождении ребенка. Расположение энцефалоцеле очень важно, так как есть определенные клинические последствия для лечения и прогноза для переднего и заднего энцефалоцеле. Задние энцефалоцеле чаще связаны с неврологическими проблемами. Энцефалоцеле передней части черепа обычно не содержат мозговой ткани и, как правило, имеют лучший прогноз.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">&nbsp;</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Наиболее распространенной областью черепа для развития энцефалоцеле является верхняя часть от лба до нижней части спины черепа в области затылочной кости. Энцефалоцеле также может возникать вблизи пазух, лба и носа или около основания черепа.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Симптомы, которые могут развиться, включают:</span></p>\r\n<ul>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">задержки в достижении основных этапов развития;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">умственную отсталость;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">неспособность к обучению;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">задержки роста;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">эпилепсию;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">ухудшение зрения;</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">несогласованные произвольные движения (атаксия);</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">гидроцефалию, состояние, при котором избыток спинномозговой жидкости в черепе вызывает давление на мозг.</span></li>\r\n</ul>\r\n<p>&nbsp;</p>",
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            "icd_name": "Микроцефалия",
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            "description": "Микроцефалия – недоразвитие черепа и головного мозга, сопровождающее умственной отсталостью и неврологическими отклонениями.  \r\n ",
            "etiology": "<p>Первичной считается микроцефалия, развитие которой произошло в результате наследования ребенком дефектных генов от одного или обоих родителей. К хромосомным заболеваниям относятся: </p>\r\n<ul>\r\n<li>Синдром Дауна; </li>\r\n<li>Синдром Эдвардса;  </li>\r\n<li>Синдром Патау; </li>\r\n<li>Синдром кошачьего крика и т.д. </li>\r\n</ul>\r\n<p>Вторичная микроцефалия развивается в результате воздействия неблагоприятных факторов в период эмбрионального развития плода, когда происходит закладка и формирование структур головного мозга. Генетический аппарат родителей при этом не нарушен. </p>\r\n<p>Вторичная микроцефалия может быть обусловлена: </p>\r\n<ul>\r\n<li>Вирусными заболеваниями (краснухой, цитомегалией, корью); </li>\r\n<li>Токсоплазмозом; </li>\r\n<li>Злоупотреблением алкоголем; </li>\r\n<li>Злоупотреблением наркотиками; </li>\r\n<li>Приемом некоторых медикаментов; </li>\r\n<li>Голоданием; </li>\r\n<li>Внутриутробной гипоксией плода; </li>\r\n<li>Механическими травмами. </li>\r\n</ul>",
            "pathogenesis": "<p>При первичной микроцефалии возникает остановка роста мозга (и вслед за ним черепа) без указаний на дегенеративный процесс или повреждение. Истинная микроцефалия всегда имеет наследственный характер. Она возникает в результате раннего пора­жения зародышевых клеток и обусловленного этим искаженного развития мозга. При этом отсутствуют признаки перенесенных мозговых заболеваний.  </p>\r\n<p>Вторичная (ложная, или церебропатическая) микро­цефалия возникает в результате рано перенесенного мозгового заболевания. Чаще оно носит воспалительный или травматиче­ский характер. </p>",
            "diagnostics": "<p>Диагностика микроцефалии включает: </p>\r\n<p>Жалобы и анамнез: уменьшение размеров головы, задержка в психоречевом развитии, снижение мышления, памяти, внимания, расторможенность, неусидчивость. Перинатальный анамнез отягощен, в анамнезе возможны перенесенные нейроинфекции. Окружность черепа не увеличивается или увеличивается незначительно. <br /> Физикальное обследование: маленькая окружность головы, лоб скошен, затылок уплощен, отмечается выраженная диспропорция между лицевым и мозговым черепом, большие выступающие уши. У 95% больных отмечается неврологическая симптоматика: нарушение мышечного тонуса, спастические парезы, судороги, умственная отсталость, расстройство координации движений, косоглазие. <br /> Инструментальные исследования: на ЭЭГ задержка формирования возрастной корковой ритмики, диффузные изменения электрогенеза головного мозга. </p>",
            "treatment": "<p>Современное лечение микроцефалии заключается в основном в симптоматической поддержке больного при помощи медикаментозных препаратов, а также в комплексных реабилитационных мероприятиях, направленных на максимальную адаптацию и социализацию ребенка. В качестве лекарственной терапии для лечения микроцефалии применяются препараты, улучшающие обменные процессы в мозговой ткани, витаминные комплексы и т. д. По показаниям - противосудорожные и седативные препараты. В рамках реабилитационных мероприятий детям с микроцефалией необходимы занятия лечебной физкультурой, массаж, трудотерапия.</p>",
            "prevention": "<p>Профилактика микроцефалии у детей предусматривает тщательное планирование беременности, обследование на инфекции (TORCH-комплекс, ПЦР), антенатальную охрану плода. Раннее внутриутробное выявление микроцефалии является основанием для решения вопроса об искусственном прерывании беременности. Медико-генетическое консультирование семей, имеющих детей с микроцефалией, необходимо для оценки потенциального риска при последующих беременностях.</p>",
            "clinical_picture": "<p>Объем черепа у ребенка с микроцефалией уменьшен уже при рождении, в дальнейшем его развитие заметно отстает от возрастной нормы. Отмечается преобладание лицевого черепа над мозговым. Типичный внешний вид больного с микроцефалией характеризуется узким и скошенным лбом, выступающими надбровными дугами, большими ушами. Большой родничок и черепные швы закрываются уже в первые месяцы жизни. В дальнейшем больные с микроцефалией обычно отстают в массе и росте (вплоть до карликовости), имеют диспропорциональное телосложение, узкое высокое (готическое) небо, большие редкие зубы. </p>\r\n<p>Неврологические нарушения при микроцефалии могут включать мышечную дистонию, спастические парезы, атаксию, судороги, косоглазие. Часто дети с микроцефалией могут страдать эпилепсией и детским церебральным параличом. Дети с микроцефалией поздно начинают держать головку, сидеть, ползать, ходить. Отмечается грубая задержка речевого развития, нечеткость артикуляции, резкая ограниченность словарного запаса, нарушение понимания обращенной речи. </p>\r\n<p>Степень интеллектуальных нарушений  у ребенка с микроцефалией может варьировать от дебильности до идиотии. При нерезко выраженной умственной отсталости больные с микроцефалией могут быть обучаемы, способны к самообслуживанию и выполнению несложных поручений. Однако в большинстве случаев дети с микроцефалией требуют ухода, контроля и надзора со стороны взрослых. </p>\r\n<p>По особенностям темперамента дети с микроцефалией могут быть отнесены к торпидной или эретической группе. В первом случае детям свойственна малоподвижность, вялость, безучастность к окружающему, пассивно-подражательная деятельность; во втором случае – гиперактивность, суетливость, подвижность, неустойчивое внимание. Эмоциональная сфера у больных с микроцефалией остается относительно сохранной: дети приветливы, добродушны; реже - эмоционально неустойчивы и склонны к аффективным вспышкам. </p>",
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            "name": "Врожденная гидроцефалия",
            "icd_name": "Врожденная гидроцефалия",
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            "slug": "q03_vrozhdennaya_gidrocefaliya",
            "lead": "Нарушение здоровья, относящееся к группе врожденные аномалии [пороки развития] нервной системы",
            "description": " \r\nВрожденная гидроцефалия – это патологическое состояние, которое сопровождается накоплением спинномозговой жидкости в желудочках мозга из-за ее избыточной продукции, нарушения всасывания или препятствие на пути оттока. ",
            "etiology": "<p>К причинам врожденной гидроцефалии относятся пороки развития ликворной системы : </p>\r\n<ul>\r\n<li>атрезия отверстий, соединяющих желудочки мозга (Мажанди и Люшка); </li>\r\n<li>дефекты в строении подпаутинного пространства; </li>\r\n<li>сужение (стеноз) сильвиевого водопровода;  </li>\r\n<li>краниовертебральные аномалии (аномалии границы между основанием черепа и верхнешейным отделом позвоночника) - аномалия Киари, врожденная базилярная импрессия. </li>\r\n</ul>\r\n<p>Причинами врожденной гидроцефалии могут также быть внутриутробные инфекции (токсоплазмоз, врожденный сифилис, цитомегалия, краснуха), родовая травма. </p>",
            "pathogenesis": "<p>Традиционно модель гидроцефалии трактуется как дисбаланс между продуцированием и абсорбцией черепно-мозговой жидкости. Современные исследования показывают, что основная роль определяется абсорбцией капиллярами мозга. Гемодинамический патогенез гидроцефалии (первичная и вторичная) определяется нарушением венозного оттока (обструктивная гидроцефалия) и уменьшением артериальной пульсации (сообщающаяся гидроцефалия).</p>",
            "diagnostics": "<p>Гидроцефалия может быть выявлена у плода в перриод внутриутробного развития при проведении скрининга беременной женщины. УЗИ плода позволяет обнаружить гидроцефалию у ребенка на 16–20 неделе беременности. После рождения у некоторых детей гидроцефалия выявляется сразу в родильном доме специалистом-неонатологом. </p>\r\n<p>Трансиллюминация (диафаноскопия) черепа позволяет выявить наружную гидроцефалию у детей, исключить гидроанэнцефалию и субдуральную гигрому.  Суть его в просве­чивании головы пучком света от лампы в затемнённом помещении. В их лучах при гидро­цефалии начинает светиться вся голова. </p>\r\n<p>Рентгенография черепа – выявляют истончение костной ткани, расхождение швов черепа, на внутренней поверхности черепной коробки присутствует характерный симптом “пальцевидных вдавлений”. </p>\r\n<p>Магнитно-резонансная и компьютерная томография позволяют с большой точностью визуализировать патологические изменения внутри черепа, выявить место, которое препятствует оттоку ликвора. </p>\r\n<p>Ультрасонография – ультразвуковое исследование головного мозга через открытый большой родничок. Позволяет определить степень повышения внутричерепного давления. </p>\r\n<p>Офтальмоскопия – осмотр глазного дна. Выявляют застойные диски зрительных нервов, как следствие повышенного внутричерепного давления. </p>\r\n<p>Для оценки давления цереброспинальной жидкости, исследования ее состава и проведения ликвородинамических проб прибегают к вентрикулярной и люмбальной пункциям.  </p>",
            "treatment": "<p>Основными принципами лечения гидроцефалии у детей является снижение продукции спиномозговой жидкости и нормализация ее циркуляции по ликвороносным путям, в т. ч. с помощью создания обходных анастомозов. </p>\r\n<p>С целью снижения продукции ликвора и внутричерепного давления проводится дегидратационная терапия диуретиками, ингибиторами карбоангидразы, салуретиками. При прогрессирующем нарастании гидроцефалии у детей в течение 2—3-х месяцев ставится вопрос о хирургическом вмешательстве. </p>\r\n<p>Оптимальный способ оперативного вмешательства определяется этиологией, формой, стадией гидроцефалии у детей. В настоящее время все виды операций при гидроцефалии у детей могут быть поделены на 5 групп: </p>\r\n<ul>\r\n<li>паллиативные вмешательства, позволяющие временно снизить внутричерепное давление и устранить краниоцеребральную диспропорцию (люмбальные и вентрикулярные пункции, наружное вентрикулярное дренирование) </li>\r\n<li>операции, направленные на подавление ликворопродукции (клипирование, коагуляция сосудистого сплетения) </li>\r\n<li>операции, направленные на восстановление естественных путей циркуляции ликвора или создание новых путей ликворооттока (удаление опухолей, внутричерепных гематом , вентрикулостомия) </li>\r\n<li>операции, активизирующие ликворосорбцию (рассечение арахноидальных спаек и др.) </li>\r\n<li>шунтирующие операции, предусматривающие отведение ликвора в другие системы организма (вентрикулоперитонеальное шунтирование, люмбоперитонеальное шунтирование, вентрикулоатриарное шунтирование, вентрикулоцистерностомия, кистовентрикулоперитонеостомия, субдуроперитонеостомия). При невозможности выполнения стандартных шунтриующих операций проводятся атипичные шунтирующие вмешательства - вентрикулоплевральное, вентрикулоуретральное вентрикулобиллиарное шунтирование. Ликворошунтирующие операции при гидроцефалии у детей сопряжены с риском нарушения функционирования дренажных систем, гипердренированием или осложнениями воспалительного характера.  </li>\r\n</ul>",
            "prevention": "<p>Чтобы предупредить развитие врожденной гидроцефалии  необходимо: </p>\r\n<ul>\r\n<li>Защищаться от инфекционных заболеваний во время беременности </li>\r\n<li>Не принимать никаких медикаментов во время беременности, кроме тех, которые прописал врач </li>\r\n<li>Профилактическое плановое УЗИ-обследование беременных женщин и нейроультрасонография у младенцев. </li>\r\n</ul>",
            "clinical_picture": "<p>У детей из-за большой податливости костей черепа не наблюдается повышения внутричерепного давления, гидроцефалия у них сопровождается увеличением размеров черепа. У новорожденных и детей раннего возраста гидроцефалия характеризуется слишком большим размером головы, выбуханием вен скальпа, напряжением и отсутствием пульсации большого родничка, отеком дисков зрительных нервов. Часто отмечается симптом «заходящего солнца» - ограничение движений глазных яблок кверху. Может наблюдаться расхождение швов черепа. Постукивание по черепу сопровождается характерным звуком (симптом «треснутого горшка»). У детей первого года жизни гидроцефалия приводит к отставанию в физическом и умственном развитии. Они позже начинают держать голову, переворачиваться, сидеть и ходить. </p>\r\n<p>Дети, у которых имеется выраженная гидроцефалия, отличаются шарообразной формой головы, ее слишком большим размером, глубоко посаженными глазами, оттопыренными ушами, истончением кожи головы. Может отмечаться снижение зрения, повышение мышечного тонуса в нижних конечностях, нарушения со стороны черепных нервов. Дети, страдающие гидроцефалией, малоподвижны, не могут следить глазами за родителями. Они раздражены, часто плачут, постоянно сонливы, плохо едят. Их часто тошнит. </p>",
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}