McGarry J, Garg B, Silbert S
Acta Neurol Scand. 1983 Jul;68(1):61-3. doi: 10.1111/j.1600-0404.1983.tb04817.x.
Two siblings with facio-scapulo-humeral dystrophy (FSH) had muscle biopsy with light microscopy and histochemistry performed. Rapid disease progression resulted in the death of one child at age 5 years. Such an outcome has not been previously reported.