伴有21-羟化酶缺乏的“获得性”肾上腺增生与先天性肾上腺增生并非同一遗传疾病。
"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.
作者信息
New M I, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine L S
出版信息
J Clin Endocrinol Metab. 1979 Feb;48(2):356-9. doi: 10.1210/jcem-48-2-356.
PMID:218988
Abstract
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.
摘要
对一名因21-羟化酶缺乏导致“获得性”肾上腺增生（AAH）患者的家族进行了激素研究和HLA基因分型。这些研究结果表明，“AAH”与先天性肾上腺皮质增生症（CAH）并非同一种遗传病。
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