{"id":12322,"date":"2024-10-11T23:34:11","date_gmt":"2024-10-11T21:34:11","guid":{"rendered":"https:\/\/valintermed.com\/?p=12322"},"modified":"2024-10-11T23:34:11","modified_gmt":"2024-10-11T21:34:11","slug":"okulodentodigitalnaya-displaziya-dominantnaya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/dominant-oculodentodigital-displasia\/","title":{"rendered":"Oculodentodigital dysplasia dominant"},"content":{"rendered":"
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Oculodentodigital dysplasia (ODD) is a rare inherited disorder classified as autosomal dominant. It is characterized by multiple developmental abnormalities affecting the ocular structures, dental tissues, and distal phalanges of the fingers. Clinically, the disease may present with various abnormalities, such as macrognathia, epicanthus, and specific changes in the structure of the teeth, including enamel hypoplasia and premature loss. Finger lesions may present as hypoplastic changes and nail abnormalities. The manifestations of the disease are very diverse and may vary in severity, making diagnosis difficult at early stages.<\/p>\n

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