{"id":12321,"date":"2024-10-11T23:34:38","date_gmt":"2024-10-11T21:34:38","guid":{"rendered":"https:\/\/valintermed.com\/?p=12321"},"modified":"2024-10-11T23:34:38","modified_gmt":"2024-10-11T21:34:38","slug":"okulodentodigitalnaya-displaziya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/okulodentodigitalnaya-displaziya\/","title":{"rendered":"Oculodentodigital dysplasia"},"content":{"rendered":"
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Oculodentodigital dysplasia (ODD) is a rare genetic disorder that belongs to the group of dysplasias characterized by abnormalities in the development of teeth, eyes, and fingers. The disease is a consequence of mutations in the genes responsible for the formation and development of these structures. ODD can manifest itself in varying degrees of severity and include clinical symptoms such as enamel hypoplasia, mysodontia (lack of teeth), abnormalities in finger growth and shape, and various eye abnormalities, including microphthalmia and coloboma. This disease is most often inherited in an autosomal dominant manner, although sporadic cases are possible.<\/p>\n

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