Definition:
Schmitt Gillenwater Kelly Syndrome is a rare disease classified as an autosomal dominant syndrome. This rare syndrome is characterized by radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema. Individuals afflicted with Schmitt Gillenwater Kelly Syndrome usually have thumbs that look like a finger and short radial bone. Males suffering from this syndrome have an abnormally positioned urethral opening. Other afflicted patients may exhibit the presence of a condition known as Prognathism, wherein one jaw is larger than the other, which eventually causes the other jaw to protrude in front of the other one.
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schmittgillenwaterkellysyndrome
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