Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci

Am J Med Genet A. 2013 Jan;161A(1):218-24. doi: 10.1002/ajmg.a.35695. Epub 2012 Dec 14.

Abstract

Distal 15q25.2 microdeletions have recently been reported as a copy number variation (CNV) locus for neurodevelopmental and neuropsychiatric disorders with variable outcome. In addition, more proximal microdeletions of 15q25.2 have been described as a susceptibility locus for cognitive deficits, congenital diaphragmatic hernia (CDH), and Diamond-Blackfan anaemia (DBA). We describe two patients with 15q25.2 deletion, one with the more distal deletion and the other with a deletion overlapping both the distal and proximal 15q25.2 deletions and compare them to the 18 so far reported patients with 15q25.2 deletions. We provide a characterization of the 15q25.2 microdeletions and contribute to the genotype-phenotype delineation for these two novel microdeletion syndromes.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Abnormalities, Multiple / physiopathology
  • Anemia, Diamond-Blackfan / genetics
  • Anemia, Diamond-Blackfan / physiopathology
  • Child
  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 15 / genetics
  • Gene Deletion
  • Genetic Association Studies
  • Genetic Loci*
  • Genotype
  • Germany
  • Hernia, Diaphragmatic / genetics
  • Hernia, Diaphragmatic / physiopathology
  • Hernias, Diaphragmatic, Congenital
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Microarray Analysis
  • Phenotype

Supplementary concepts

  • Chromosome 15q, partial deletion