Volume 243, Number 10, 700-705, DOI: 10.1007/BF00873975

Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I

Lorenzo Pavone, Agata Fiumara, Rita Barone, Renata Rizzo, Piera Buttitta, William B. Dobyns and Jaak Jaeken

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Abstract

The carbohydrate-deficient glycoprotein (CDG) syndromes are a group of genetic multisystem disorders with invariable involvement of the nervous system including severe olivopontocerebellar atrophy. We report two sets of sibs in whom the diagnosis of CDG syndrome type 1 was recognized at an older age because of marked olivopontocerebellar atrophy seen on MRI. Previous CT findings were interpreted as showing Dandy-Walker malformation. Three of the patients are also among the oldest reported with this syndrome.

Key words  Carbohydrate-deficient glycoprotien syndromme - Olivopontocerebellar atrophy

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