Lissencephaly with cerebellar hypoplasia type A

Orpha code: 100011OMIM code:

Definition

A rare, genetic, lissencephaly with cerebellar hypoplasia subtype characterized by classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable, predominantly midline, cerebellar hypoplasia.

Disease data
Classification

Malformation syndrome

ORPHA code
100011
OMIM code
-
ICD10 code
Q04.3
ICD11 code
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl