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| Year : 1997 | Volume
: 45
| Issue : 3 | Page : 193--195 |
Infantile facioscapulohumeral muscular dystrophy with Coat俟Q製 syndrome.
SK Tamer, S Jain, S Hiran
Department of Neurosciences, JLN Hospital and Research Centre, Bhilai - 490 006, Madhya Pradesh, India
Correspondence Address:
SK Tamer
Department of Neurosciences, JLN Hospital and Research Centre, Bhilai - 490 006, Madhya Pradesh
India
A case of facioscapulohumeral dystrophy (FSH) with several unusual feature is being presented. It俟Q製 early onset in infancy as against commonly occurring onset in second decade, the relentless progressive course without abortive or apparent arrest phase as is often seen, the calf hypertrophy, marked skeletal changes and associated retinal changes seen in Coat俟Q製 disease are the noteworthy features of this unusual case.
How to cite this article:
Tamer S, Jain S, Hiran S. Infantile facioscapulohumeral muscular dystrophy with Coat's syndrome. Neurol India 1997;45:193-195
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How to cite this URL:
Tamer S, Jain S, Hiran S. Infantile facioscapulohumeral muscular dystrophy with Coat's syndrome. Neurol India [serial online] 1997 [cited 2023 Mar 27 ];45:193-195
Available from: https://www.neurologyindia.com/article.asp?issn=0028-3886;year=1997;volume=45;issue=3;spage=193;epage=195;aulast=Tamer;type=0 |
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