Infant with classic congenital adrenal hyperplasia (CAH) born to a mother with classic cah

Todd D. Nebesio, Nerissa C. Kreher, Tamara S. Hannon

Research output: Contribution to journalArticle

Abstract

We report a female infant with classic congenital adrenal hyperplasia (CAH), secondary to 21-hydroxylase deficiency, who was born to a mother with salt-wasting CAH.

Original languageEnglish (US)
Pages (from-to)250-252
Number of pages3
JournalJournal of Pediatrics
Volume145
Issue number2
DOIs
StatePublished - Aug 1 2004

Keywords

  • 17-hydroxyprogesterone
  • 17-OHP
  • ACTH
  • Adrenocorticotropic hormome
  • CAH
  • Congenital adrenal hyperplasia

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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