[A case of complete triploidy (69,XXY) in a premature infant. Presence of a clinical syndrome characteristic of this chromosome abnormality]

Ann Pediatr (Paris). 1976 Oct 2;23(10):639-45.
[Article in French]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / epidemiology
  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosomes, Human, X / genetics*
  • Chromosomes, Human, Y / genetics*
  • Cryptorchidism / genetics
  • Cytogenetics
  • Disorders of Sex Development / genetics
  • Fatal Outcome
  • Humans
  • Infant, Newborn
  • Infant, Premature, Diseases / diagnosis
  • Infant, Premature, Diseases / epidemiology
  • Infant, Premature, Diseases / genetics*
  • Karyotyping
  • Male
  • Placenta / abnormalities
  • Polyploidy*
  • Rare Diseases
  • Registries
  • Risk Factors
  • Sex Chromatin / genetics
  • Syndactyly / genetics