{"id":12343,"date":"2024-10-11T23:12:54","date_gmt":"2024-10-11T21:12:54","guid":{"rendered":"https:\/\/valintermed.com\/?p=12343"},"modified":"2024-10-11T23:12:54","modified_gmt":"2024-10-11T21:12:54","slug":"orofatsiodigitalnyy-sindrom-2-go-tipa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/orofaciodigital-syndrome-type-2\/","title":{"rendered":"Orofaciodigital syndrome type 2"},"content":{"rendered":"
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Orofaciodigital syndrome type 2 (OFDDS 2) is a rare genetic disorder characterized by a complex of abnormalities affecting the face, arms, and legs. The disorder results from mutations in genes responsible for tissue development and formation, resulting in a variety of dysmorphic and functional disorders. Patients with OFDS 2 may exhibit a wide range of symptoms, including abnormalities in the structure of teeth, changes in the shape and size of fingers, and facial abnormalities such as cleft lip or palate. The need for a multidisciplinary approach in treatment and rehabilitation makes this disorder relevant to doctors of various specialties, from geneticists to orthopedists and dentists.<\/p>\n

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