A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy
P. H. P. Jansen, E.M.G. Joosten, H. H. J. Jaspar, H.M. Vingerhoets
Abstract
P. H. P. Jansen, E.M.G. Joosten, H. H. J. Jaspar, H.M. Vingerhoets
Abstract
Three patients from a large pedigree are described who had autosomal dominant spinal muscular atrophy that became manifest between the end of the fourth and the sixth decade. The disease progressed rapidly without evidence of corticospinal tract dysfunction, and within 3 years the patients died from respiratory failure.
OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Three patients from a large pedigree are described who had autosomal dominant spinal muscular atrophy that became manifest between the end of the fourth and the sixth decade. The disease progressed rapidly without evidence of corticospinal tract dysfunction, and within 3 years the patients died from respiratory failure.
Key concepts: Spinal muscular atrophy, Medicine, Progressive muscular atrophy, Atrophy, Corticospinal tract, Physical medicine and rehabilitation, Anatomy, Disease