Literature DB >> 2277390

Familial congenital laryngeal abductor paralysis: different expression in a family with one male and three females affected.

A Schinzel1, E Hof, P Dangel, W Robinson.   

Abstract

A brother and two sisters of remotely consanguineous parents had congenital laryngeal abductor paralysis and moderate mental retardation. In the two older sibs, mental deficiency could have resulted from birth asphyxia, but the youngest girl was already microcephalic at birth and had no apparent asphyxia. The mother, who was healthy and of normal intelligence, was found on laryngoscopy to have unilateral laryngeal abductor paralysis. This is the first family with both mentally retarded and nonretarded affected members with congenital laryngeal abductor paralysis. Inheritance is most likely autosomal dominant with variable expression, but autosomal recessive inheritance, with both parents carriers and the mother an affected homozygote, and X linked inheritance are also possible.

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Year:  1990        PMID: 2277390      PMCID: PMC1017266          DOI: 10.1136/jmg.27.11.715

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  7 in total

1.  CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

Authors:  D PLOTT
Journal:  N Engl J Med       Date:  1964-09-17       Impact factor: 91.245

2.  Hereditary abductor vocal cord paralysis.

Authors:  R R Gacek
Journal:  Ann Otol Rhinol Laryngol       Date:  1976 Jan-Feb       Impact factor: 1.547

3.  Familial laryngeal abductor paralysis and psychomotor retardation.

Authors:  G V Watters; N Fitch
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

4.  Familial laryngeal abductor paralysis with presumed autosomal dominant inheritance.

Authors:  G Morelli; C Mesolella; F Costa; B Testa; V Ventruto; S Santulli
Journal:  Ann Otol Rhinol Laryngol       Date:  1982 May-Jun       Impact factor: 1.547

5.  Autosomal dominantly inherited adductor laryngeal paralysis--a new syndrome with a suggestion of linkage to HLA.

Authors:  M Mace; E Williamson; D Worgan
Journal:  Clin Genet       Date:  1978-11       Impact factor: 4.438

6.  Autosomal dominant inheritance of Gerhardt's syndrome in three generations of a family.

Authors:  G Morelli; C Mesolella; M L Cavaliere; M Stabile; V Ventruto
Journal:  J Med Genet       Date:  1980-08       Impact factor: 6.318

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

Authors:  F X Brunner; I F Herrmann
Journal:  Laryngol Rhinol Otol (Stuttg)       Date:  1982-04
  7 in total
  1 in total

1.  A RAPGEF6 variant constitutes a major risk factor for laryngeal paralysis in dogs.

Authors:  Sheida Hadji Rasouliha; Laura Barrientos; Linda Anderegg; Carina Klesty; Jessica Lorenz; Lucie Chevallier; Vidhya Jagannathan; Sarah Rösch; Tosso Leeb
Journal:  PLoS Genet       Date:  2019-10-24       Impact factor: 5.917

  1 in total

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