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[Familial recurrent laryngeal nerve paralysis, a genetically fixed syndrome -- additional remark on linkage of deficiency gene and HLA (author's transl)].

作者信息

Brunner F X, Herrmann I F

出版信息

Laryngol Rhinol Otol (Stuttg). 1982 Apr;61(4):186-8.

PMID:7098715
Abstract

Hereditary laryngeal paralysis has been rarely reported. Some authors describe additional neurological signs in connection with the cranial nerve, or mental retardation. It has been assumed that there is a causal connection with genetic deficiency. Familial studies, presented with this article, showed abductor and adductor paralysis in the mother and in the son, aged 13, abductor paralysis in the daughters, who were 11 and 5 years old, respectively, and normal laryngeal function in the father and in one 10-year old daughter. There were no neurological signs or mental deficits in any member of the family. Genetic analysis of blood-group and HLA systems confirmed linkage of the HLA system and vocal cord disorder, as suggested by Mace et al. (5). Hence, further observations and investigations will be necessary to prove this statement.

摘要

相似文献

1
[Familial recurrent laryngeal nerve paralysis, a genetically fixed syndrome -- additional remark on linkage of deficiency gene and HLA (author's transl)].
Laryngol Rhinol Otol (Stuttg). 1982 Apr;61(4):186-8.
2
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[Experimental study on simultaneous selective reinnervation of the adductors and the abductor muscle for the treatment of the laryngeal paralysis].[内收肌与外展肌同步选择性再支配治疗喉麻痹的实验研究]
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引用本文的文献

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PLoS Genet. 2019 Oct 24;15(10):e1008416. doi: 10.1371/journal.pgen.1008416. eCollection 2019 Oct.
2
Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected.家族性先天性喉外展肌麻痹:在一个有一名男性和三名女性患病的家族中的不同表现。
J Med Genet. 1990 Nov;27(11):715-6. doi: 10.1136/jmg.27.11.715.