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"lead": "Нарушения зрения — снижение способности видеть до такой степени, что вызывает проблемы, не устраняемые обычными способами, такими как очки или лекарства.[1][2][3]\r\n\r\nЭто может быть из-за болезни, травмы, врождённых или дегенеративных заболеваний. Эта потеря зрения, как правило, определяется как:\r\n\r\nОстрота зрения с коррекцией менее 20/60, или значительный дефект центрального поля,\r\nЗначительный одноимённый или разноимённый двусторонний визуальный дефект периферического поля, включающий дефект поля или общее сжатия или сужение поля, или\r\nПониженный пик контрастной чувствительности с любым из указанных выше условий.[1][2][3][4]\r\nГлазные нарушения, которые могут привести к нарушениям зрения могут включать в себя дегенерацию сетчатки, альбинизм, катаракты, глаукомы, мышечные проблемы, которые приводят к нарушениям зрения, расстройства роговицы, диабетическую ретинопатию, врождённые пороки и инфекции. Нарушения зрения также могут быть вызваны расстройствами мозга и нервной системы, в этом случае их, как правило, называют кортикальными нарушениями зрения (CVI). Путеводитель оценки постоянного ухудшения американской медицинской ассоциации попытался представить «стандартизированный, объективный подход к оценке медицинских нарушений». Глава Визуальная система «устанавливает критерии для оценки постоянного ухудшения зрительной системы, как это влияет на способность человека выполнять действия в повседневной жизни».[5] Путеводитель оценил, что потеря одного глаза составляет 25 % нарушений зрительной системы и 24 % от полного обесценивания человека;[5][6]. Полная потеря зрения на оба глаза, как считается, является 100 % нарушением зрения и 85 % от полного обесценивания человека[5]\r\n\r\nВизуальные нарушения наносят значительный экономический удар даже в развитых странах.[7] Значительную часть глобального нарушения зрения можно предупредить.",
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"code": "H27.0",
"name": "Афакия",
"icd_name": "Афакия",
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"slug": "h27.0_afakiya",
"lead": "патологическое состояние глаза, которое характеризуется отсутствием хрусталика",
"description": "",
"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;\">Афакия хрусталика бывает врожденной и приобретенной. Для первой формы заболевания характерно первоначальное отсутствие хрусталиковой линзы. На это могут влиять следующие причины:</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;\">генетические нарушения, не позволяющие обособиться тканям хрусталика;</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;\">внешние и внутренние причины, которые вызывают рассасывание образованного хрусталика у плода. Когда зарождается контакт роговицы и хрусталика, появляется задержка развития структур глазного яблока. Это приводит к образованию первичной формы врожденной афакии. Для развития вторичной формы характерно спонтанное рассасывание хрусталика. </span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </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 формы встречаются достаточно редко в отличие от приобретенных. В зависимости от локализации заболевания афакия делится на монокулярную и бинокулярную: при развитии первой страдает один глаз, во втором случае наступает афакия обоих глаз.</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;\">В случае приобретенной патологии могут возникать различные причины потери хрусталика:</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;\">глубокая травма или контузия глазного яблока;</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;\">хирургическое удаление катаракты. </span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p> </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;\">Риск появления афакии в результате травмы существует в любом возрасте.</span></p>",
"pathogenesis": "",
"diagnostics": "<p> </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;\">Кроме общего осмотра глаз, диагностика афакии требует проведения целого ряда специальных исследований органа зрения: биомикроскопии глаза, визометрии, гониоскопии, рефрактометрии, офтальмоскопии и УЗИ.Визометрия показан всем пациентам, она выявляет степень ухудшения остроты зрения, что необходимо перед проведением коррекции. Проведение гониоскопии выявляет увеличение глубины передней камеры глаза. Офтальмоскопия позволяет обнаружить сопутствующие патологии и выбрать тактику дальнейшего лечения. </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;\">Коррекция афакии проводится при помощи очков, контактных и интраокулярных линз. Показанием к очковой коррекции зрения является двухсторонняя форма заболевания. При односторонней афакии очки рекомендованы только при непереносимости контактных методов коррекции. Выбор стекла для эмметропичного глаза затруднен, т. к. даже стекло в +10 диоптрий не сопоставимо с преломляющей силой хрусталика, которая равняется 19 диоптриям. Это обусловлено тем, что коэффициент преломления жидкости, которая окружает хрусталик, выше, чем воздушной среды, окружающей стекло.</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;\">Оптическая сила стеклянной линзы зависит от рефракции пациента. При гиперметропии необходимо подобрать очки с более сильной оптикой, чем при миопии. Нет необходимости в назначении методов коррекции зрения пациентам с высокой степенью миопии до удаления хрусталика. В связи с отсутствием способности к аккомодации пациенту следует назначить очки для работы на близком расстоянии на 3,0 диоптрий сильнее, чем для дальнего видения.</span></p>\r\n<p> </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;\">Контактная или интраокулярная коррекция зрения показаны пациентам с монокулярной афакией. Назначение очков пациентам с данной формой заболевания будет усугублять анизейконию. В ходе оперативного вмешательства (интраокулярной коррекции) проводится имплантация искусственной линзы с индивидуально подобранной оптической силой. Наиболее предпочтительным вариантом лечения является использование заднекамерных линз, т. к. локализируясь в месте расположения естественной линзы, они обеспечивают высокое качество зрения. Врожденную афакию при помощи данной методики можно корректировать только после достижения ребенком двухлетнего возраста.</span></p>",
"prevention": "<p> </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;\">Специфические меры, способные предотвратить врожденную афакию, в офтальмологической практике отсутствуют. С целью предотвращения случаев приобретенной афакии следует ежегодно проходить офтальмологический осмотр, которые поможет своевременно диагностировать сложные заболевания приводящие к вынужденному хирургическому удалению хрусталика. Лицам, имеющим высокий риск получения травм глаза из-за особенностей профессиональной деятельности, обязательно использовать в работе средства защиты – маски и очки.</span></p>",
"clinical_picture": "<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;\">Специфическим симптомом афакии является иридодонез (дрожание радужки), который развивается при движении глаз. При обследовании у пациентов отмечается снижение остроты зрения и способности к аккомодации. В прогностическом плане наиболее неблагоприятной является односторонняя форма заболевания, так как клиническая картина осложняется анизейконией. Индуцированная органической патологией аномалия сопровождается различием в размере изображения на сетчатке глаз, вследствие чего резко ухудшается бинокулярное зрение.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </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;\">Врожденная форма патологии характеризуется прогрессирующим снижением остроты зрения при относительной стабильности остальных клинических проявлений. Отсутствие своевременного лечения может стать причиной слепоты. Для послеоперационной формы афакии свойственна стадийность течения основного заболевания, которое послужило причиной проведения оперативного вмешательства по удалению хрусталика. Клиническая картина травматической афакии характеризуется прогрессирующим нарастанием симптоматики, ранними проявлениями которой являются интенсивный болевой синдром с нарастанием местного отека и прогредиентное снижение остроты зрения.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </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;\">Из астенопических жалоб у пациентов с афакией отмечается появление тумана перед глазами, низкая способность к фиксации и двоение изображения. Неспецифическими проявлениями заболевания являются головная боль, общая слабость, повышенная раздражительность.</span></p>\r\n<p> </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;\">Врожденная форма афакии или удаление хрусталика в детском возрасте осложняется микрофтальмией. При полном отсутствии капсулы хрусталика стекловидное тело ограничено только пограничной мембраной. Это служит причиной формирования грыжи стекловидного тела. В случае разрыва пограничной мембраны содержимое стекловидного тела выходит в переднюю камеру глаза. В то же время контактная коррекция является провоцирующим фактором развития кератита, образования рубцов на роговице, в роговично-склеральной области и лимбе.</span></p>",
"image": null,
"image_alt": null,
"standard_type": 0,
"danger": 40,
"published": 1,
"parent": 6453,
"block_rubric": 78,
"standards": []
},
{
"id": 10701,
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"name": "Ретиношизис и ретинальные кисты",
"icd_name": "Ретиношизис и ретинальные кисты",
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"lead": "патологическое изменение сетчатки, при котором наблюдается разделение ретинальных слоев на наружный (хориоидальный) и внутренний (витреальный)",
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"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;\">Выделяют три формы ретиношизиса:</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;\">Дегенеративный ретиношизис. Является приобретённой формой заболевания. Возникает в возрасте после 40 лет вследствие дистрофических изменений в сетчатой оболочке глаза. Встречается в двух формах – типичный и ретикулярный (отличается большим размером кист в ретине).</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;\">Наследственный ретиношизис. Развивается в результате генетических нарушений. Может быть сцепленным с Х-хромосомой, передаваться по аутосомно-доминантному или рецессивному типу. Иногда является одним из симптомов генетически обусловленных патологий, таких как болезнь Гольдмана-Фавре или Вагнера.</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;\">Вторичный ретиношизис. Возникает при сосудистых заболеваниях глаз (диабетическая ретинопатия, тромбоз центральной вены сетчатки), воспалительных процессах (хронические формы увеита, иридоциклита), травмах органа зрения, онкологических заболеваниях сосудистой оболочки, в результате воздействия некоторых лекарственных препаратов.</span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>",
"pathogenesis": "<p> </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;\">В основе патогенеза ретиношизиса лежит нарушение кровообращения в макулярной области и на периферии сетчатки. Нарушения в сетчатке проявляются в виде кистозной дегенерации. Слияние образовавшихся кист способствует образованию больших полостей внутри сетчатки, расслаивающих ретину на всем ее протяжении. Зона расслоения может оставаться целой, но может и разрываться в одном или даже обоих листках. Это приводит к развитию отслойки сетчатки и гибели ретинальных структур.</span></p>",
"diagnostics": "<p> </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;\">Для диагностики ретиношизиса используют базовые методы обследования: визиометрию, тонометрию, офтальмоскопию с использованием щелевой лампы и линзы Гольдмана. Для уточнения диагноза дополнительно назначают УЗИ глазного яблока, электроретинографию (для определения функционального состояния сетчатки), флюоресцентную ангиографию (для диагностики патологии в макуле, при врожденном ретиношизисе). Компьютерная периметрия помогает установить наличие дефектов в поле зрения. Оптическая когерентная томография является ведущим методом при данной патологии. Позволяет точно выявить изменения в макулярной области сетчатки, определить наличие кист и отслоек на периферии.</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;\">Определение тактики лечения заболевания сетчатки осуществляет офтальмолог, который учитывает локализацию патологических процессов, стадию их развития, риск осложнений и индивидуальные показатели пациента. В процессе применяют консервативные и хирургические методики. Первые направлены на стимуляцию обменных процессов и циркуляции крови в ретине и предусматривают приём витаминов, антиоксидантов и нейрометаболических стимуляторов. Курс лечения нужно проводить регулярно, каждые шесть месяцев. Фармакологические препараты вводят в вену или мышцу.</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;\">Что касается хирургических методик, то они представлены лазерной коагуляцией или такой операцией, как витрэктомия, направленными на то, чтобы остановить патологические процессы.</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;\">Лазерная коагуляция позволяет исключить риск отслоения ретины за счёт её прижигания в областях соединения с хориоидеей. После применения такого лечения многие пациенты отмечают существенное повышение остроты зрения.</span></p>\r\n<p> </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;\">Витрэктомия направлена на частичное или полное удаление стекловидного тела и его замещение газом или специально разработанной жидкостью. Такой подход позволяет восстановить внутренние глазные структуры и исключить риск развития осложнений.</span></p>",
"prevention": "<p> </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;\">Профилактика ретиношизиса заключается в регулярном посещении врача-офтальмолога, особенно после 40 лет. При наличии миопии высокой степени необходимо максимально исключить тяжелые физические нагрузки, стрессовые ситуации на работе и дома. При открытоугольной глаукоме необходимо регулярно применять назначенные капли и контролировать ВГД каждые 3 месяца. При повышении артериального давления рекомендуется принимать лекарственные препараты для его коррекции. Следует избегать травм глаза и головы. Регулярное посещение врача-офтальмолога и точное соблюдение его рекомендаций существенно снижает риск осложнений при ретиношизисе и способствует длительной стабилизации заболевания.</span></p>",
"clinical_picture": "<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;\">Дегенеративный ретиношизис обычно протекает бессимптомно. Патология выявляется случайно во время профилактических осмотров у врача-офтальмолога. Проявляется поражением на уровне наружного плексиформного слоя ретинальной оболочки. Первичные изменения возникают на крайней нижневисочной периферии и характеризуются образованием обширных участков с мелкокистозной дистрофией в слоях ретины. При распространении процесса на макулу или при развитии отслойки сетчатки появляются жалобы на снижение остроты зрения, сужение полей зрения, искажение предметов, появление вспышек перед глазами.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </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;\">Наследственный ретиношизис чаще диагностируется в возрасте 7-9 лет. Макулярная область поражается в первую очередь, в результате появляются жалобы на снижение центрального зрения (трудности при чтении, письме, просмотре телевизора). Повреждение локализуется на уровне клеток Мюллера, в результате чего слой нервных волокон отслаивается от остальной части сетчатой оболочки. Периферические нарушения в сетчатой оболочке при ретиношизисе чаще всего локализуются в нижневисочном квадранте, проявляются развитием гигантских овальных кист с последующим формированием отслойки. Поражение двустороннее.</span></p>\r\n<p> </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;\">Вторичный ретиношизис является осложнением различных заболеваний глазного яблока. Клинические проявления зависят от основной патологии. Из осложнений ретиношизиса выделяют развитие обширных отслоек в сетчатой оболочке глаза, кровоизлияния под ретину, в кисты расслоенной оболочки или в стекловидное тело.</span></p>",
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{
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