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Oro-facial-digital syndrome type II with otolaryngological manifestations
A Havle1, S Shedge2, S Malashetti1
1Department of ENT, Krishna Institute of Medical Sciences University, Karad, Maharashtra, India.
Abstract:
We present a case of oro-facial-digital syndrome type II (Mohr's syndrome) which is characterized by malformations of the oral cavity, face and digits. The facial and oral features include tongue nodules, cleft or high-arched palate, missing teeth, broad nose; cleft lip. The digital features include clinodactyly, polydactyly, syndactyly, brachydactyly and duplication of the hallux.
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