Related Experiment Video
Updated: Aug 16, 2026

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
Published on: July 29, 2007
The Lewis family revisited: no evidence for autosomal dominant multiple system atrophy
José Berciano1, Gregor K Wenning
1Department of Neurology, University Hospital Marqués de Valdecilla (UC), Santander, Spain.
Abstract:
In 1964, Lewis reported a familial ataxia-dysautonomia syndrome reminiscent of Shy-Drager syndrome subsequently known as multiple system atrophy (MSA). Here we review this report and propose that the Lewis family may represent an unusual form of autosomal dominant cerebellar ataxia type I, which might be categorized either as SCA3 (Machado-Joseph disease) or a new SCA subtype. There remains no conclusive evidence to support the notion of hereditary MSA.
Related Concept Videos
Multiple Sclerosis l: Introduction
Myasthenia Gravis ll: Pathophysiology
Lysosomal Hydrolases
Pedigree Analysis
Parkinson Disease ll: Pathophysiology
Alterations in Muscle Tone lll

