Lissencephaly with cerebellar hypoplasia type B

Orpha code: 100012OMIM code:

Definition

A form of lissencephaly with cerebellar hypoplasia characterized by subtle microcephaly, hypotonia and neurological and cognitive development delay. Hippocampal malformation is a characteristic imaging feature of this disorder.

Disease data
Classification

Malformation syndrome

ORPHA code
100012
OMIM code
-
ICD10 code
Q04.3
ICD11 code
-

No additional description.

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