Heterotaxy with left atrial isomerism in a patient with deletion 18p

Am J Med Genet. 2000 Sep 18;94(3):198-200. doi: 10.1002/1096-8628(20000918)94:3<198::aid-ajmg4>3.0.co;2-9.

Abstract

We report on a female infant with partial deletion of the short arm of chromosome 18 (del 18p) and heterotaxy with left atrial isomerism. Congenital heart defect (CHD) is found in 10% of the literature reports. Interestingly, situs abnormalities have been diagnosed in four patients with del 18p, including ours. This finding could imply that a locus or loci involved in the development of normal body situs lies within this chromosomal region. Del 18p must be consid- ered when evaluating a patient with phenotypic anomalies and CHD in lateralization defects.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 18*
  • Female
  • Heart Atria / abnormalities*
  • Heart Defects, Congenital / genetics*
  • Humans
  • Infant