Oculodental syndrome, Rutherfurd type
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.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
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Oculodental syndrome, Rutherfurd type?
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