{"id":12824,"date":"2024-09-17T21:43:13","date_gmt":"2024-09-17T19:43:13","guid":{"rendered":"https:\/\/valintermed.com\/?p=12824"},"modified":"2024-09-17T21:43:13","modified_gmt":"2024-09-17T19:43:13","slug":"sindrom-retta","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/retta-syndrome\/","title":{"rendered":"Rett syndrome"},"content":{"rendered":"
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Rett syndrome is a rare neurological disorder that primarily affects girls and appears in the first two years of life. The disorder is caused by mutations in the MECP2 gene, which disrupts normal brain development. The syndrome is characterized by developmental regression, loss of communication and motor skills, and the appearance of stereotypical movements. Rett syndrome is usually diagnosed after the child has had normal early development, making it especially difficult for parents and doctors to diagnose. Symptoms include loss of skills, delayed psychomotor development, and respiratory and motor disorders.<\/p>\n

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