A Syndrome with Juvenile Cataract, Cerebellar Atrophy, Mental Retardation and Myopathy
- 1 August 1987
- journal article
- research article
- Published by Georg Thieme Verlag KG in Neuropediatrics
- Vol. 18 (03) , 164-169
- https://doi.org/10.1055/s-2008-1052473
Abstract
Four patients of two families with clinical characteristics resembling those in Marinesco-Sjögren syndrome are presented. All patients had infantile hypotonia as the presenting sign. In preschool age ataxia, cataract and mental retardation manifested. CT scan revealed cerebellar atrophy. Muscle biopsy showed myopathic changes with vacuolar degeneration and marked adipose tissue proliferation. Electron microscopy showed myelin bodies and autophagic vacuoles. The conclusion is that the peculiar myopathic and degenerative findings in the muscle biopsy are a consistent morphological feature in the clinical entity of the patients and the syndrome is distinctive from Marinesco-Sjögren syndrome.Keywords
This publication has 3 references indexed in Scilit:
- Autosomal recessive distal muscular dystrophy: A comparative study with distal myopathy with rimmed vacoule formationAnnals of Neurology, 1985
- Sensorimotor Neuropathy in a Patient with Marinesco-Sjögren SyndromeEuropean Neurology, 1983
- LE SYNDROME DE MARINESCO-SJOGREN PREMIERE ETUDE ANATOMO-CLINIQUE1965