Literature DB >> 3775291

Hereditary congenital facial paralysis.

J P Nicolai, M Y Bos, B G ter Haar.   

Abstract

Hereditary congenital facial paralysis is rare. This paper presents a pedigree of four generations of a family of about 100 members, nine of whom suffer from congenital facial paresis, three with impaired hearing, and three with both facial paresis and impaired hearing. Heredity is dominant with reduced penetrance.

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Year:  1986        PMID： 3775291     DOI： 10.3109/02844318609006289

Source DB:  PubMed          Journal:  Scand J Plast Reconstr Surg        ISSN： 0036-5556


  2 in total

1.  A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

Authors:  H T Verzijl; B van den Helm; B Veldman; B C Hamel; L P Kuyt; G W Padberg; H Kremer
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

Review 2.  Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'.

Authors:  K D MacDermot; R M Winter; D Taylor; M Baraitser
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318
  2 in total

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