12q14 microdeletion syndrome and short stature with or without relative macrocephaly

Am J Med Genet A. 2012 Oct;158A(10):2542-4. doi: 10.1002/ajmg.a.35527. Epub 2012 Aug 10.

Abstract

Patients with 12q14 microdeletion can present with short stature with or without relative macrocephaly. When associated with relative macrocephaly, the phenotype resembles Silver-Russell syndrome (SRS). Short stature is attributable to haploinsufficiency of HMGA2, but a patient with a deletion at the HMGA2 locus only did not have macrocephaly. Hence, the presence of a separate locus for a relative macrocephaly phenotype was suggested. Herein, we present a girl with a 12q14 microdeletion involving the HMGA2 locus who had short stature but did not have macrocephaly. Inclusion and exclusion mappings based on a quantitative review of the degree of relative macrocephaly and the extent of the deletions in previously reported patients with a 12q14 microdeletion demonstrated a presumptive interval for relative macrocephaly spanning a few megabases. These results confirm that a deletion spanning both HMGA2 and this presumptive interval locus would cause an SRS-like phenotype.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion*
  • Chromosome Disorders / genetics*
  • Chromosome Disorders / pathology*
  • Chromosomes, Human, Pair 12 / genetics*
  • Dwarfism / genetics*
  • Female
  • HMGA2 Protein / genetics*
  • Humans
  • Megalencephaly / genetics
  • Megalencephaly / pathology*
  • Phenotype
  • Silver-Russell Syndrome / genetics
  • Silver-Russell Syndrome / pathology

Substances

  • HMGA2 Protein