{"id":11878,"date":"2025-07-25T20:56:38","date_gmt":"2025-07-25T18:56:38","guid":{"rendered":"https:\/\/valintermed.com\/?p=11878"},"modified":"2025-07-25T20:56:38","modified_gmt":"2025-07-25T18:56:38","slug":"lissentsefaliya-2","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/lissentsefaliya-2\/","title":{"rendered":"Lissencephaly 2"},"content":{"rendered":"
<\/div>\n

Lissencephaly is a rare neurological disorder characterized by an abnormality of the cerebral cortex in which the normal sulci are absent or greatly reduced. This results in abnormal brain development and significant neurological and psychiatric disorders. The disease can manifest itself in varying degrees of severity, from mild mental retardation to severe disability. Lissencephaly can be either primary or secondary, and may result from genetic disorders, viral infections during pregnancy, and other predisposing factors. Recognizing and understanding this disorder is key to diagnosis and subsequent treatment, which is especially important in infants and young children who may have severe developmental delays.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n