Lissencephaly I

Lissencephaly I

*Gene map locus 17p13.3

ILS

LIS1

Lissencephaly sequence, isolated

Lissencephaly, classic

SBH

SCLH

Subcortical band heterotopia

Subcortical laminar heterotopia

[Clinical features: brain malformation; epilepsy; mental retardation]


LIS1-Related Isolated Lissencephaly	LIS1-Related Isolated Lissencephaly	LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
Archives of Neurology	Archives of Neurology	Human Molecular Genetics


LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation	The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene	Type I Lissencephaly
Human Molecular Genetics	Human Molecular Genetics	Indian Pediatrics


Coronal US image of a 34-week fetus with type I lissencephaly shows the absence of the cingulate sulcus from the expected location (arrow) on the medial hemispheric surface
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Edited by Aldo Campana, August 21, 2012