Congenital Combined Pituitary Hormone Deficiency Attributable to a Novel PROP1 Mutation (467insT)

J Pediatr Endocrinol Metab. 2023 Nov 2;19(4):491-498. doi: 10.1515/jpem-2006-190406. Print 2006 Apr 1.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Female
  • Homeodomain Proteins* / genetics
  • Humans
  • Hypopituitarism* / genetics
  • Male
  • Mutation*
  • Prognosis