[Spongious cerebral dystrophy at an infant age (Canavan-Bogaert-Bertrand types) in three siblings of a non-Jewish family in upper Franconia (author's transl)]

Klin Padiatr. 1978 Nov;190(6):580-5.
[Article in German]

Abstract

A daughter and two sons of possibly consangineous parents died after motor and mental deterioration at 18, 16 and 15 months of age. Spongy degeneration of the CNS (Canavan-van-Bogaert-Bertrand type) was diagnosed on neuropathological examinationtion; the histological findings were almost identical in the patients. Own clinical experiences are compared with reports from the literature; data important in clinical and differential diagnosis are reviewed. Pathogenetical and etiological aspects are discussed; autosomal recessive inheritance has to be considered in genetic counselling.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Autopsy
  • Consanguinity
  • Demyelinating Diseases / genetics
  • Diagnosis, Differential
  • Female
  • Humans
  • Infant
  • Lipidoses / diagnosis
  • Lipidoses / genetics*
  • Lipidoses / pathology
  • Male
  • Syndrome