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Robinow-Sorauf syndrome

MIM.180750

Autosomal dominant disease

Synopsis

- flat facies
- thin, long, pointed nose
- shallow orbits
- hypertelorism
- plagiocephaly (asymmetry of orbits)
- strabismus
- broad great toes
- duplicated great toe distal phalanx

Etiology

- mutations in the TWIST gene (MIM.601622)