{"id":11219,"date":"2025-07-27T05:57:06","date_gmt":"2025-07-27T03:57:06","guid":{"rendered":"https:\/\/valintermed.com\/?p=11219"},"modified":"2025-07-27T05:57:06","modified_gmt":"2025-07-27T03:57:06","slug":"semeynaya-porentsefaliya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/family-porentsefalia\/","title":{"rendered":"Familial porencephaly"},"content":{"rendered":"
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Familial porencephaly is a rare inherited disorder characterized by abnormal brain development that in most cases has severe neurological manifestations. This condition involves variations in the size and shape of brain structures, which can lead to a variety of neurological disorders, including mental retardation, speech delays, and motor delays. Familial porencephaly can be caused by a number of genetic factors and mutations, highlighting the importance of genetic counseling for individuals with a family history of the disorder.<\/p>\n

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