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

Todd Nebesio, Nerissa C. Kreher, Tamara 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
Pages (from-to)250-252
Number of pages3
JournalJournal of Pediatrics
Volume145
Issue number2
DOIs
StatePublished - Aug 2004

Fingerprint

Congenital Adrenal Hyperplasia
Mothers
Salts
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

Keywords

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

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Infant with classic congenital adrenal hyperplasia (CAH) born to a mother with classic cah. / Nebesio, Todd; Kreher, Nerissa C.; Hannon, Tamara.

In: Journal of Pediatrics, Vol. 145, No. 2, 08.2004, p. 250-252.

Research output: Contribution to journalArticle

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