Arthrogryposis Multiplex Congenita Associated with Lissencephaly: A Case Report
- 1 February 1988
- journal article
- research article
- Published by Georg Thieme Verlag KG in Neuropediatrics
- Vol. 19 (01) , 24-26
- https://doi.org/10.1055/s-2008-1052396
Abstract
A child with arthrogryposis multiplex congenita and microcephaly is described. Cranial CT-scan and MRI showed abnormalities consistent with type I lissencephaly. The lissencephaly seems to be the primary cause of the congential contractures. Lissencephaly associated with arthrogryposis multiplex congenita has to be considered as a special kind of lissencephaly syndrome.This publication has 4 references indexed in Scilit:
- Syndromes with lissencephaly. II: Walker‐Warburg and Cerebro‐Oculo‐Muscular syndromes and a new syndrome with type II lissencephalyAmerican Journal of Medical Genetics, 1985
- Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephalyAmerican Journal of Medical Genetics, 1984
- Lissencephaly (Agyria) on Computed TomographyJournal of Computer Assisted Tomography, 1979
- Lissencephaly in 2 siblingsNeurology, 1963