Literature DB >> 3955865

A family with congenital suprabulbar paresis (Worster-Drought syndrome).

M A Patton, M Baraitser, E M Brett.   

Abstract

A three generation family is described in which four members were found to have congenital suprabulbar paresis (Worster-Drought syndrome). It is suggested that some cases of congenital suprabulbar paresis are inherited as an autosomal dominant trait with variable expression and penetrance.

Entities:  

Mesh:

Year:  1986        PMID: 3955865     DOI: 10.1111/j.1399-0004.1986.tb01239.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Electromagnetic function of polymicrogyric cortex in congenital bilateral perisylvian syndrome.

Authors:  R Paetau; J Saraneva; O Salonen; L Valanne; J Ignatius; S Salenius
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-05       Impact factor: 10.154

2.  Worster-Drought Syndrome Associated With LINS Mutations.

Authors:  Hugh J McMillan; Anne-Lise Holahan; Julie Richer
Journal:  Child Neurol Open       Date:  2018-08-02
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.