Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study

Neuropediatrics
A A KroonR C Hennekam

Abstract

A newborn with a rare type of lissencephaly is reported, characterized by extreme cerebral and cerebellar hypoplasia. The diagnosis was made by postmortem magnetic resonance imaging, indicating the value of such studies to evaluate neuronal migration disorders in patients in whom autopsy cannot be performed. Two earlier described microlissencephaly syndromes, the "Barth" and "McComb" type, are reviewed.

Citations

May 20, 1998·Pediatric Neurology·L SztrihaM Varughese
Aug 14, 2013·BMC Veterinary Research·Valentín PérezJuan José Arranz
Oct 11, 2005·Journal of Neuropathology and Experimental Neurology·Mark S FormanJeffrey A Golden
Jul 26, 2014·Acta Neuropathologica Communications·Catherine Fallet-BiancoNadia Bahi-Buisson
Dec 14, 1999·American Journal of Medical Genetics·B KernerW B Dobyns
Aug 2, 2008·Brain : a Journal of Neurology·Catherine Fallet-BiancoFiona Francis
Apr 26, 2017·American Journal of Medical Genetics. Part a·Nataliya Di DonatoWilliam B Dobyns
Feb 13, 2018·Continuum : Lifelong Learning in Neurology·John Gaitanis, Tomo Tarui

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