Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing

A. Kauschansky*, H. Kaufman, R. Zamir, E. Elian

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

ACTH stimulation tests and HLA genotyping were performed on the family of a patient with late onset adrenal hyperplasia due to 21-hydroxylase deficiency (21-OH-def). The results of these studies suggest that homozygous members of the family are clinically normal. Our family data confirm that late onset adrenal hyperplasia due to 21-OH-def is linked to HLA.

Original languageEnglish
Pages (from-to)73-78
Number of pages6
JournalHormone Research in Paediatrics
Volume14
Issue number2
DOIs
StatePublished - 1981

Keywords

  • 17-OH progesterone
  • Adrenal hyperplasia
  • HLA

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