Oculodental syndrome, Rutherfurd type

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Synonyms: Gingival hypertrophy-corneal dystrophy | Rutherfurd syndrome

Oculodental syndrome Rutherfurd type is a rare genetic disorder that is primarily characterized by the classical triad of gingival fibromatosis non-eruption of tooth and corneal dystrophy (bilateral corneal vascularization and opacity). Abnormally shaped teeth have also been reported. The syndrome is transmitted as an autosomal dominant trait.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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