{"id":12971,"date":"2024-08-23T07:25:02","date_gmt":"2024-08-23T05:25:02","guid":{"rendered":"https:\/\/valintermed.com\/?p=12971"},"modified":"2024-08-23T07:25:02","modified_gmt":"2024-08-23T05:25:02","slug":"sindrom-smita-magenisa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sick-person-syndrome\/","title":{"rendered":"Smith-Magenis syndrome"},"content":{"rendered":"
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Smith\u2013Magenis syndrome (SMS) is a rare genetic disorder caused by a deletion or mutation in the RAI1 gene. The disorder is characterized by multiple abnormalities, including intellectual disability, specific physical features, behavioral problems, and sleep disorders. Clinical manifestations of the syndrome include hypotonia, delays in psychomotor development, and severe impairments in communication and socialization. The main facial features of patients may include short stature, a broad nasal bridge, and characteristic ear shapes. Smith\u2013Magenis syndrome is also associated with a variety of comorbid conditions, which can complicate diagnosis and treatment. <\/p>\n

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