Skeletal anomalies in genetically determined congenital heart disease

Radiol Clin North Am. 1971 Dec;9(3):435-58.
No abstract available

MeSH terms

  • Abnormalities, Multiple / diagnostic imaging
  • Adolescent
  • Adult
  • Arm / abnormalities
  • Body Constitution
  • Bone Diseases
  • Bone Diseases, Developmental / complications*
  • Bone and Bones / abnormalities*
  • Child
  • Child, Preschool
  • Chromosome Aberrations
  • Chromosome Disorders
  • Cleft Palate / complications
  • Craniosynostoses / complications
  • Ellis-Van Creveld Syndrome / complications
  • Face / abnormalities
  • Female
  • Fingers / abnormalities
  • Heart Defects, Congenital / complications
  • Heart Defects, Congenital / diagnostic imaging
  • Heart Defects, Congenital / genetics*
  • Humans
  • Hypercalcemia / complications
  • Hypogonadism / complications
  • Infant
  • Infant, Newborn
  • Intellectual Disability / complications
  • Klippel-Feil Syndrome / complications
  • Laurence-Moon Syndrome / complications
  • Lentigo / complications
  • Male
  • Marfan Syndrome / complications
  • Obesity / complications
  • Pierre Robin Syndrome / complications
  • Radiography
  • Radius / abnormalities
  • Scoliosis / complications
  • Thrombocytopenia / complications
  • Toes / abnormalities
  • Turner Syndrome / complications