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Journal of Clinical Endocrinology & Metabolism Vol. 48, No. 2 356-359
doi:10.1210/jcem-48-2-356
Copyright © 1979 by the Endocrine Society.
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"ACQUIRED" ADRENAL HYPERPLASIA WITH 21-HYDROXYLASE DEFICIENCY IS NOT THE SAME GENETIC DISORDER AS CONGENITAL ADRENAL HYPERPLASIA

M.I New, F Lorenzen, S Pang, P Gunczler, B Dupont and L.S Levine

The Division of Pediatric Endocrinology, Department of Pediatrics, The New York Hospital-Cornell Medical Center, New York, N.Y. 10021, and The Tissue Typing Laboratory, Sloan-Kettering Institute for Cancer Research New York, N.Y. 10021

Hormonal studies and HLA genotyping were performed on the family of a patient with "acquired" adrenal hyperplasia (AAH) due to 21-hydroxylase deficiency. The results of these studies suggest that "AAH", is not the same genetic disease as CAH.




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