PMID: 2495176Feb 1, 1989Paper

Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome

Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery
M SasakiT Nagano

Abstract

A Japanese male infant with lissencephaly, congenital muscular dystrophy (CMD), and ocular abnormalities is described. This patient represents features of the cerebro-oculo-muscular syndrome. Cranial computerized tomography revealed diffuse agyria, low density of the white matter, and hypoplasia of the cerebellar vermis. Brain histology suggested type II lissencephaly. These findings are correlated with other similar conditions, such as Walker-Warburg syndrome, Fukuyama-type CMD, and muscle, eye and brain disease.

References

Sep 1, 1987·European Journal of Pediatrics·M Warburg
Jan 1, 1984·Acta Neuropathologica·J TowfighiR L Ladda
Jul 1, 1984·American Journal of Medical Genetics·W B DobynsF Greenberg
Jul 1, 1984·Journal of Neuropathology and Experimental Neurology·K TakadaJ Tanaka

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Citations

Apr 1, 1993·Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery·A M LaverdaR Casellato
Aug 1, 1993·International Ophthalmology·D G Sanders, C M Mooy
Apr 1, 1992·Journal of Child Neurology·J D CookM Banna
Mar 1, 1995·Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery·J F Martínez-LageT Rodriguez Costa
Jun 1, 1991·Child's Nervous System : ChNS : Official Journal of the International Society for Pediatric Neurosurgery·J F Martínez-LageF Hidalgo

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