2 top medical experts on Oculodental syndrome Rutherfurd syndrome across 1 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Oculodental syndrome 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Corneal dystrophy with gum hypertrophy, Gingival Hypertrophy With Corneal Dystrophy, Gingival hypertrophy corneal dystrophy, Rutherfurd syndrome
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