Oculodental syndrome, Rutherfurd type

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.

Also known as: Rutherfurd syndrome, corneal dystrophy with gum Hypertrophy, corneal dystrophy with gum hypertrophy, gingival Hypertrophy with corneal dystrophy, gingival hypertrophy corneal dystrophy, gingival hypertrophy-corneal dystrophy

0 clinical trials for this condition and its sub-types, 0 tagged with Oculodental syndrome, Rutherfurd type itself.