ISCA-37421-Loss

1q21.1 recurrent region (BP3-BP4, distal) (includes GJA5) Loss
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
dysmorphic features, 612474, Moderate mental retardation, microcephaly, cardiac abnormalities, and cataracts, mild to moderate developmental delay