Literature DB >> 6651132

Ocular manifestations of congenital muscular dystrophy (Fukuyama type).

T Chijiiwa, M Nishimura, H Inomata, T Yamana, O Narazaki, T Kurokawa.   

Abstract

Ocular manifestations in two cases of congenital muscular dystrophy of Fukuyama type were reported. This disease is characterized by early onset of hypotonia, generalized muscle weakness and atrophy, mental retardation, and elevated serum creatine-phosphokinase activity. The symptoms include entropion of lower lids, pathological myopia with astigmatism, optic nerve pallor, and irregular grayish subretinal mottling. Case 1 showed additional features of posterior staphyloma, dragged papillomacular vessels, peripheral grayish-white discoloration of the retina, and rete mirabile as well as abnormal vascular anastomosis.

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Mesh:

Year:  1983        PMID: 6651132

Source DB:  PubMed          Journal:  Ann Ophthalmol        ISSN: 0003-4886


  4 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.  Ocular findings in Walker-Warburg syndrome.

Authors:  H Gerding; F Gullotta; K Kuchelmeister; H Busse
Journal:  Childs Nerv Syst       Date:  1993-11       Impact factor: 1.475

3.  Neuropathological findings in muscle-eye-brain disease (MEB-D). Neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama type.

Authors:  Q H Leyten; K Renkawek; W O Renier; F J Gabreëls; C M Mooy; H J ter Laak; R A Mullaart
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

4.  Cerebro-ocular dysplasia-muscular dystrophy (COD-MD) syndrome.

Authors:  J Towfighi; J W Sassani; K Suzuki; R L Ladda
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

  4 in total

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