Asplenia in ATR-X syndrome: a second report

Am J Med Genet A. 2005 Nov 15;139(1):37-9. doi: 10.1002/ajmg.a.30990.

Abstract

Mutation at the ATR-X locus is associated with severe mental retardation. Several conditions, initially reported as clinically distinct phenotypes, have now been attributed to ATR-X mutation. Asplenia, in association with severe mental retardation, has been reported and subsequently demonstrated in one family to be due to ATR-X mutation. We now report on a second instance of a patient presenting with mental retardation and asplenia who has been shown to have a mutation at the ATR-X locus.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple*
  • DNA Helicases / genetics*
  • Humans
  • Infant, Newborn
  • Intellectual Disability / genetics
  • Male
  • Mutation
  • Nuclear Proteins / genetics*
  • Pneumococcal Infections / etiology
  • Spleen / abnormalities*
  • Syndrome
  • X-linked Nuclear Protein

Substances

  • Nuclear Proteins
  • DNA Helicases
  • ATRX protein, human
  • X-linked Nuclear Protein