Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.

Gerkes, Erica H

Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion. [electronic resource] - European journal of medical genetics - 344-6 p. digital

Publication Type: Case Reports; Journal Article

1878-0849

10.1016/j.ejmg.2010.05.003 doi


Cerebral Cortex--abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 22
Developmental Disabilities--genetics
DiGeorge Syndrome--genetics
Humans
Infant
Intellectual Disability--genetics
Magnetic Resonance Imaging
Male
Malformations of Cortical Development--genetics
Microcephaly--genetics