Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

Hum Genet. 1984;65(4):317-9. doi: 10.1007/BF00291554.


Partial monosomy of 22q due to an unbalanced 4;22 translocation was seen in a 2-month-old male with Type I truncus arteriosus, dysmorphic features, and T-cell abnormalities. The family history revealed a previous sib with Type I truncus arteriosus, thymic aplasia, and parathyroid hypoplasia noted on postmortem examination, consistent with DiGeorge syndrome. Evaluation of the asymptomatic mother of these two patients revealed partial T-cell deficiency and the same unbalanced translocation with deletion of proximal 22q11. These findings provide further evidence that some cases of complete or partial DiGeorge syndrome are associated with monosomy of the proximal long arm of chromosome 22, and they may explain many, if not all, familial cases of the syndrome.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aneuploidy*
  • Chromosome Banding
  • Chromosomes, Human, 21-22 and Y*
  • Chromosomes, Human, 4-5
  • DiGeorge Syndrome / genetics*
  • Female
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Infant
  • Karyotyping
  • Male
  • Translocation, Genetic*