X-Linked Spinal and Bulbar Muscular Atrophy of Late Onset (Kennedy-Stefanis Disease?)
- 1 January 1981
- journal article
- research article
- Published by S. Karger AG in European Neurology
- Vol. 20 (6) , 485-488
- https://doi.org/10.1159/000115283
Abstract
X-linked spinal and bulbar muscular atrophy of late onset is a rare variety of motor neuron disease. In this report a Greek family with 2 affected brothers is described. It is interesting that all Greek cases of this disease originate from a small group of Greek islands. Transient fatigue is an additional feature of the disease which is manifested sometimes before other symptoms are apparent. The progression of the disease appears to be faster than in spinal muscular atrophy of Wohlfart-Kugelberg-Welander. Regarding the name of this disorder, we propose the descriptive term, ‘X-linked spinal and bulbar muscular atrophy of late onset’ or ‘Kennedy-Stefanis disease’.Keywords
This publication has 2 references indexed in Scilit:
- Motoneuropathie héréditaire: La forme proximale de l'adulte liéé au sexe (ou maladie de kennedy)Journal of the Neurological Sciences, 1979
- Progressive proximal spinal and bulbar muscular atrophy of late onsetNeurology, 1968