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 language | English |
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Pages (from-to) | 73-78 |
Number of pages | 6 |
Journal | Hormone Research in Paediatrics |
Volume | 14 |
Issue number | 2 |
DOIs | |
State | Published - 1981 |
Keywords
- 17-OH progesterone
- Adrenal hyperplasia
- HLA