Neuropediatrics 1987; 18(3): 164-169
DOI: 10.1055/s-2008-1052473
© Georg Thieme Verlag KG Stuttgart · New York

A Syndrome with Juvenile Cataract, Cerebellar Atrophy, Mental Retardation and Myopathy

Riitta  Herva1 , L. von Wendt1 , Gunvor von Wendt1 , Anna-Liisa  Saukkonen1 , J.  Leisti1 , V.  Dubowitz2
  • 1Departments of Pathology, Paediatrics, Ophthalmology and Clinical Genetics, Oulu University Central Hospital, Oulu, Finland
  • 2Department of Paediatrics and Neonatal Medicine, Hammersmith Hospital, London, England
Further Information

Publication History

Publication Date:
15 May 2008 (online)

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.

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