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X-linked recessive inheritance in a family with isolated congenital alopecia

✍ Scribed by Hidemi Anzai; Hiroshi Shimizu; Takeji Nishikawa


Book ID
118561001
Publisher
The Lancet
Year
1996
Tongue
English
Weight
336 KB
Volume
347
Category
Article
ISSN
0140-6736

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A new X-linked recessive deafness syndrome was recently reported and mapped to Xq22 (Mohr-Tranebjaerg syndrome). In addition to deafness, the patients had visual impairment, dystonia, fractures, and mental deterioration. The female carriers did not have any significant manifestations of the syndrome