Literature DB >> 3995786

Autosomal recessive congenital cerebellar hypoplasia.

A Wichman, L M Frank, T E Kelly.   

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.

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Year:  1985        PMID: 3995786     DOI: 10.1111/j.1399-0004.1985.tb02279.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  A new case of complete primary cerebellar agenesis: clinical and imaging findings in a living patient.

Authors:  Feng Yu; Qing-jun Jiang; Xi-yan Sun; Rong-wei Zhang
Journal:  Brain       Date:  2014-08-22       Impact factor: 13.501

2.  Sex-linked recessive congenital ataxia.

Authors:  I D Young; J R Moore; J H Tripp
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-09       Impact factor: 10.154

3.  Subtotal agenesis of the cerebellum in an adult. MRI demonstration.

Authors:  R N Sener; J R Jinkins
Journal:  Neuroradiology       Date:  1993       Impact factor: 2.804

4.  MRI in cerebellar hypoplasia.

Authors:  N deSouza; R Chaudhuri; J Bingham; T Cox
Journal:  Neuroradiology       Date:  1994       Impact factor: 2.804

  4 in total

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