{"id":12036,"date":"2025-03-14T00:20:06","date_gmt":"2025-03-13T23:20:06","guid":{"rendered":"https:\/\/valintermed.com\/?p=12036"},"modified":"2025-03-14T00:20:06","modified_gmt":"2025-03-13T23:20:06","slug":"meningoentsefalotsele","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/meningo-entrepreneurial\/","title":{"rendered":"Meningoencephalocele"},"content":{"rendered":"
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Meningoencephalocele is a rare neurogenetic disorder characterized by the formation of a defect in the skull or spinal cord with the effusion of meninges and nervous tissue into the resulting sac. This condition occurs as a result of abnormal development of the fetus during the first trimester of pregnancy, which leads to a violation of the closure of the neural tube. Meningoencephalocele can manifest itself in various forms, depending on the location and size of the resulting transparent sac. Defects can vary from small seals on the surface of the skull to extensive tumor-like formations. Clinical manifestations can include neurological disorders such as hydrocephalus, epileptic seizures, and psychomotor retardation. The characteristic clinical picture and the need for immediate surgical intervention determine the importance of early diagnosis and a comprehensive approach to the treatment of this rare disease.<\/p>\n

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