X pentasomy: a case and review

Hum Genet. 1979 Nov 1;52(1):69-77. doi: 10.1007/BF00284599.

Abstract

A 49,XXXXX girl is reported. The most typical features of the patient are: severe mental retardation, serious dental anomalies, various anomalies of the bones, and a high rate of gonadotropins. The few similar cases so far described are reviewed to aid in delineation of this rare syndrome. The implications of Lyon's hypothesis on X-aneuploidies are also discussed.

Publication types

  • Case Reports

MeSH terms

  • Aneuploidy*
  • Bone and Bones / abnormalities
  • Child
  • Female
  • Follicle Stimulating Hormone / blood
  • Humans
  • Intellectual Disability / genetics
  • Luteinizing Hormone / blood
  • Sex Chromosome Aberrations / genetics*
  • Syndrome
  • Tooth Abnormalities / genetics
  • X Chromosome

Substances

  • Luteinizing Hormone
  • Follicle Stimulating Hormone