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| Year : 1997 | Volume
: 45
| Issue : 3 | Page : 193--195 |
Infantile facioscapulohumeral muscular dystrophy with Coat's 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
 Source of Support: None, Conflict of Interest: None  | Check |
PMID: 29512548 
A case of facioscapulohumeral dystrophy (FSH) with several unusual feature is being presented. It's 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's disease are the noteworthy features of this unusual case.
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