Literature DB >> 7279823

Familial late onset oculopharyngeal muscular dystrophy.

D A Isenberg, P Kahn.   

Abstract

An English family is described several members of which have suffered from oculopharyngeal muscular dystrophy. No symptoms were noticed in any affected members of the family until aged at least 50 years. An autosomal dominant pattern of inheritance is clearly shown.

Entities:  

Mesh：

Substances：

Year:  1981        PMID： 7279823      PMCID： PMC2424787          DOI： 10.1136/pgmj.57.663.41

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN： 0032-5473            Impact factor:   2.401


  5 in total

Review 1.  MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.

Authors:  J N WALTON
Journal:  Br Med J       Date:  1964-05-16

2.  OCULAR MYOPATHY WITH DYSPHAGIA.

Authors:  G M BRAY; M KAARSOO; R T ROSS
Journal:  Neurology       Date:  1965-07       Impact factor: 9.910

3.  Oculopharyngeal muscular dystrophy. A familial disease of late life characterized by dysphagia and progressive ptosis of the evelids.

Authors:  M VICTOR; R HAYES; R D ADAMS
Journal:  N Engl J Med       Date:  1962-12-20       Impact factor: 91.245

4.  Progressive dystrophy of the external ocular muscles (ocular myopathy).

Authors:  L G KILOH; S NEVIN
Journal:  Brain       Date:  1951       Impact factor: 13.501

5.  Atypical muscle mitochondria in oculoskeletal myopathy.

Authors:  J A Morgan-Hughes; W G Mair
Journal:  Brain       Date:  1973-06       Impact factor: 13.501
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.