A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndrome

Clin Genet. 1990 Jul;38(1):74-8. doi: 10.1111/j.1399-0004.1990.tb03550.x.

Abstract

The authors report a patient affected with mental retardation, dysarthria, bilateral testicular hypoplasia and extensive ulcers of the lower limbs. Clinical study and laboratory tests revealed 48,XXYY syndrome. The authors confirm the importance of differential diagnosis from Klinefelter syndrome, illustrating the parameters and the pathology of both syndromes. They discuss the hypotheses concerning the pathogenesis of the ulcerations, and stress the importance of clinical and genetic characterization, leading to a differentiated prognosis of social capacity and prospect of working.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Angiography
  • Chromosome Banding
  • Diagnosis, Differential
  • Humans
  • Karyotyping
  • Klinefelter Syndrome / diagnosis
  • Leg Ulcer / blood
  • Leg Ulcer / diagnostic imaging
  • Leg Ulcer / etiology*
  • Male
  • Platelet Aggregation
  • Sex Chromosome Aberrations / diagnosis*
  • Sex Chromosome Aberrations / genetics
  • Sex Chromosome Aberrations / pathology
  • X Chromosome*
  • Y Chromosome*