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一种以常染色体显性性状遗传的进行性感音神经性耳聋和白内障综合征。

A syndrome of progressive sensorineural deafness and cataract inherited as an autosomal dominant trait.

作者信息

Guala A, Germinetti V, Sebastiani F, Silengo M C

机构信息

Istituto di Discipline Pediatriche Universitá di Torino, Italy.

出版信息

Clin Genet. 1992 Jun;41(6):293-5. doi: 10.1111/j.1399-0004.1992.tb03400.x.

Abstract

In 1982, Nadol & Burgess reported a new syndrome of cataract and progressive sensorineural hearing loss, inherited in an autosomal dominant fashion. Extensive histopathologic studies of the inner ear of the proband revealed severe cochleosaccular degeneration. No other sporadic or familial cases of such a genetic syndrome have subsequently been described. We report here a second family in which the syndrome of cataract and progressive sensorineural deafness is observed in eight members, and is inherited according to an autosomal dominant pattern.

摘要

1982年,纳多尔和伯吉斯报告了一种以常染色体显性方式遗传的白内障和进行性感音神经性听力损失新综合征。对先证者内耳进行的广泛组织病理学研究显示严重的耳蜗球囊变性。此后未再描述过这种遗传综合征的其他散发性或家族性病例。我们在此报告第二个家系,该家系中有8名成员出现白内障和进行性感音神经性耳聋综合征,且按照常染色体显性模式遗传。

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