{"id":12967,"date":"2024-08-23T07:26:30","date_gmt":"2024-08-23T05:26:30","guid":{"rendered":"https:\/\/valintermed.com\/?p=12967"},"modified":"2024-08-23T07:26:30","modified_gmt":"2024-08-23T05:26:30","slug":"sindrom-singltona-mertena","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/melancholy-syndrome\/","title":{"rendered":"Singleton-Merten syndrome"},"content":{"rendered":"
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Singleton-Merten syndrome (SMS) is a rare genetic disorder characterized by multiple systemic abnormalities, including specific facial features, musculoskeletal problems, and various metabolic changes. The disorder is associated with abnormalities in gene structure, including mutations in the MSC1 gene, which leads to clinical manifestations at the level of both sex chromosomes. The syndrome usually manifests itself in childhood or adolescence and can affect the skin, hair, teeth, and joints, causing a variety of clinical symptoms and inconsistencies in the normal physiological process. Given the complexity of the disease course and the variety of symptoms, it is important to consider the individual characteristics of each patient during diagnosis and treatment.<\/p>\n

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