Pediatric Neurology Briefs
Published 1997 | Version v1.0.0
Journal Article Open

Genetics of Juvenile Spinal Muscular Atrophy

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Abstract

A 20-year-old female with difficulties in running and climbing stairs since age 10 and suspected of having spinal muscular atrophy (SMA) type III (Kugelberg-Welander disease) was diagnosed with GM2 gangliosidosis at the Department of Human Genetics, Sackler Faculty of Medicine, Tel Aviv University, and Sapir Medical Center, Kfar-Sava, Israel.

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PNB-11-46-b

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Created
1997
When the item was originally created.