Literature DB >> 12119931

A family with Möbius syndrome.

F Becker-Christensen1, H T Lund.   

Abstract

A classic Möbius syndrome, including bilateral abducens-facial paralysis, was found in a newborn boy. At least 15 maternal relatives showed partial features of the syndrome. As potential features of Möbius syndrome also were found in the father's side of the family, a recessive mode of inheritance is suggested.

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Year:  1974        PMID： 12119931     DOI： 10.1016/s0022-3476(74)80569-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


  3 in total

Review 1.  Examining the genetics of congenital facial paralysis--a closer look at Moebius syndrome.

Authors:  Sameep Kadakia; Samuel N Helman; Thomas Schwedhelm; Masoud Saman; Babak Azizzadeh
Journal:  Oral Maxillofac Surg       Date:  2015-02-10

2.  Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndrome.

Authors:  J Herrmann; P D Pallister; E F Gilbert; C Vieseskul; E Bersu; J C Pettersen; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-04-06       Impact factor: 3.183

Review 3.  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
  3 in total

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