{"id":11273,"date":"2025-07-27T03:24:38","date_gmt":"2025-07-27T01:24:38","guid":{"rendered":"https:\/\/valintermed.com\/?p=11273"},"modified":"2025-07-27T03:24:38","modified_gmt":"2025-07-27T01:24:38","slug":"femoralno-litsevoy-sindrom","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/femoral-litsevoy-sindrom\/","title":{"rendered":"Facial femoral syndrome"},"content":{"rendered":"
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Facial femoral syndrome (FFS) is a rare genetic disorder characterized by abnormal development of the skull and facial area, as well as abnormalities of the lower limbs. This disorder is characterized by changes in the structure of bones, muscles, and soft tissues, which can lead to various functional and aesthetic defects. The most common manifestations of FFS are facial asymmetry, unlikely limb length, and joint dysplasia. Patients most often have other abnormalities, such as heart defects or respiratory disorders. Due to differences in manifestations and severity of the disease, approaches to diagnosis and treatment should be individualized.<\/p>\n

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