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扭发伴先天性耳聋(比约恩斯塔德综合征)——一个家族中三例病例报告,提示常染色体显性遗传。

Pili torti with congenital deafness (Bjornstad's syndrome)--report of three cases in one family, suggesting autosomal dominant transmission.

作者信息

Petit A, Dontenwille M M, Bardon C B, Civatte J

机构信息

Service de Dermatologie, Hôpital Saint-Louis, Paris, France.

出版信息

Clin Exp Dermatol. 1993 Jan;18(1):94-5. doi: 10.1111/j.1365-2230.1993.tb00983.x.

Abstract

Pili torti is a rare hair shaft abnormality in which the hair is flattened and intervals twisted at irregular through 180 degrees about its axis. Pili torti may occur as a congenital defect or as an acquired disorder (secondary to patchy alopecia from a variety of causes). When it is congenital, it may be isolated and determined by an autosomal dominant gene or associated with various rare syndromes, including ectodermal dysplasias, neurological defects and metabolic disturbances. The association of neurosensory hearing loss and pili torti has been recognized as Bjornstad's syndrome since 1965. As far as we know, only 15 cases of this syndrome have been reported. We describe here three cases of Bjornstad's syndrome in one family.

摘要

扭发是一种罕见的毛干异常,毛发变扁,且每隔一段就围绕其轴不规则扭转180度。扭发可作为先天性缺陷出现,也可作为后天性疾病出现(继发于各种原因导致的斑秃)。先天性扭发可能是孤立的,由常染色体显性基因决定,或与各种罕见综合征相关,包括外胚层发育不良、神经缺陷和代谢紊乱。自1965年以来,神经感觉性听力损失与扭发的关联被认为是比约恩斯塔德综合征。据我们所知,该综合征仅报告过15例。我们在此描述一个家族中的3例比约恩斯塔德综合征病例。

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