Hirschsprung disease in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome

J Pediatr. 1983 Sep;103(3):425-7. doi: 10.1016/s0022-3476(83)80422-3.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Cleft Palate / complications*
  • Disorders of Sex Development / complications*
  • Female
  • Hirschsprung Disease / complications*
  • Humans
  • Infant, Newborn
  • Microcephaly / complications*
  • Phenotype
  • Syndrome