Chromosome 22 marker in a child with Duane syndrome and urogenital abnormalities

Ann Genet. 1996;39(3):168-72.

Abstract

The nature and the origin of de novo small marker chromosome found at prenatal diagnosis were determined by fluorescence in situ hybridization (FISH) using chromosome centromere-specific probes and by chromosome in situ suppression (CISS) using chromosome specific libraries. The small marker was characterized as being derived from chromosome 22. The fetus which exhibited a minichromosome had kidney malformations and after birth showed clinical features consistent with the Duane anomaly. One previous case with Duane anomaly and abnormalities of urogenital tract associated to a bisatellitated marker derived from chromosome 22 was reported. These findings indicate that a gene or genes located in the region of chromosome 22pter-->q11 may be associated with the Duane anomaly and the development of the urogenital tract.

MeSH terms

  • Adult
  • Amniocentesis
  • Chromosomes, Human, Pair 22 / ultrastructure*
  • DNA, Satellite / genetics
  • Duane Retraction Syndrome / diagnostic imaging
  • Duane Retraction Syndrome / embryology
  • Duane Retraction Syndrome / genetics*
  • Female
  • Fetal Growth Retardation / diagnostic imaging
  • Fetal Growth Retardation / genetics
  • Fetal Growth Retardation / pathology
  • Humans
  • In Situ Hybridization, Fluorescence*
  • Infant, Newborn
  • Intellectual Disability / embryology
  • Intellectual Disability / genetics*
  • Male
  • Polycystic Kidney Diseases / diagnostic imaging
  • Polycystic Kidney Diseases / embryology
  • Polycystic Kidney Diseases / genetics*
  • Pregnancy
  • Ultrasonography, Prenatal

Substances

  • DNA, Satellite