Neurodevelopmental and immunological features in a child presenting 22q13.2 microdeletion

Am J Med Genet A. 2016 Mar;170(3):792-4. doi: 10.1002/ajmg.a.37470. Epub 2015 Nov 14.

Authors

Susanne Thümmler¹, Fabienne Giuliano², Houda Karmous-Benailly², Christian Richelme³, Arnaud Fernandez¹, Christine De Georges¹, Florence Askenazy¹

Affiliations

¹ University Department of Child and Adolescent Psychiatry, Nice Children's Hospitals CHU-Lenval, Nice, France.
² Department of Human Genetics, University Hospital of Nice, Nice, France.
³ Department of Pediatrics, Nice Children's Hospitals CHU-Lenval, Nice, France.

PMID: 26566763
DOI: 10.1002/ajmg.a.37470

No abstract available

Publication types

Case Reports

MeSH terms

Child
Chromosome Deletion*
Chromosome Mapping
Chromosomes, Human, Pair 22*
Comparative Genomic Hybridization
Facies
Female
Genetic Association Studies*
Humans
Immune System Diseases / diagnosis
Immune System Diseases / genetics
Immunoglobulin E / blood
Immunoglobulin E / immunology
Neurodevelopmental Disorders / diagnosis
Neurodevelopmental Disorders / genetics
Phenotype

Substances

Immunoglobulin E