Infantile facioscapulohumeral muscular dystrophy with Coat's syndrome

A case of Facioscapulohumeral dystrophy (FSH) with several unusual feature is being presented, It's early onset in infancy as against commonly occuring 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.