Autosomal recessive congenital cerebellar hypoplasia
- 1 April 1985
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 27 (4) , 373-382
- https://doi.org/10.1111/j.1399-0004.1985.tb02279.x
Abstract
We report three sibling pairs with congenital cerebellar hypoplasia. All six children presented in the first years of life with delays in motor and language development. All patients showed cerebellar and/or vermal dysfunction and, on formal psychometric testing, cognitive abilities ranged from normal to moderately retarded. Abnormalities on CT scan ranged from prominent valleculla to an enlarged cisterna magna with hypoplasia of the cerebellar hemispheres and vermis. The pedigrees are consistent with autosomal recessive inheritance.Keywords
This publication has 5 references indexed in Scilit:
- Human Cerebellar HypoplasiaArchives of Neurology, 1980
- Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant miceJournal of Comparative Neurology, 1973
- EARLY FAMILIAL CEREBELLAR DEGENERATION*Journal of Nervous & Mental Disease, 1950
- EARLY FAMILIAL CEREBELLAR DEGENERATION - REPORT OF 3 CASES IN ONE FAMILY1950
- PRIMARY DEGENERATION OF THE GRANULAR LAYER OF THE CEREBELLUM: AN UNUSUAL FORM OF FAMILIAL CEREBELLAR ATROPHY OCCURRING IN EARLY LIFEBrain, 1940