Literature DB >> 4003043

A Fukuyama type of congenital muscular dystrophy associated with atypical gyrate atrophy of the choroid and retina. A case report.

H Mishima, H Hirata, H Ono, K Choshi, Y Nishi, K Fukuda.   

Abstract

A three-year-ten-month old boy with the Fukuyama type of congenital muscular dystrophy (FCMD), early onset of muscular hypotonia, severe mental retardation, a slow progressive course and a characteristic fundus appearance similar to that of gyrate atrophy is described. Hyperornithinaemia and iminoglycinuria were not noted. To our knowledge, this is the first reported case of FCMD associated with atypical gyrate atrophy of the choroid and retina.

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Year:  1985        PMID: 4003043     DOI: 10.1111/j.1755-3768.1985.tb01528.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


  2 in total

1.  A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms.

Authors:  Hiroyuki Kondo; Kayoko Saito; Mari Urano; Yukiko Sagara; Eiichi Uchio; Mineo Kondo
Journal:  Jpn J Ophthalmol       Date:  2010-12-30       Impact factor: 2.447

2.  Gyrate atrophy-like phenotype with normal plasma ornithine and low plasma taurine.

Authors:  Aubhugn T Labiano; Milagros H Arroyo
Journal:  GMS Ophthalmol Cases       Date:  2020-02-27
  2 in total

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