| Literature DB >> 9929981 |
T Kondoh1, A Tsuru, T Matsumoto, T Matsuzaka, Y Tsuji.
Abstract
The disease "deafness and onychodystrophy" (DOD) is characterized by congenital hearing impairment and dystrophic or absent nails and teeth. The autosomal dominant form of the disorder has been previously reported only in one family. We describe here another family in which three members in three generations (a girl, her mother, and her maternal grandfather) were affected with DOD. Our finding is consistent with an autosomal dominant mode of inheritance and confirms autosomal dominant DOD (DDOD, MIM *124480) as a recognizable clinical entity.Entities:
Mesh:
Year: 1999 PMID: 9929981 DOI: 10.1007/s100380050109
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172