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Screening for non-classic 21-hydroxylase deficiency in an HLA-B14 positive population.

作者信息

Motta P, Airaghi L, Catania A, Mangone I, Orsatti A, Tenconi L, Cantalamessa L, Zanussi C

机构信息

Clinica Medica II, Università di Milano, Italy.

出版信息

Acta Endocrinol (Copenh). 1987 Oct;116(2):211-5. doi: 10.1530/acta.0.1160211.

Abstract

To evaluate whether HLA-B14 positive individuals are at increased risk for non-classic 21-hydroxylase deficiency, the response of progesterone and 17-hydroxyprogesterone to ACTH stimulation test was studied in a group of 27 apparently normal, HLA-B14 positive, blood donors. Four of these subjects showed a response typical of 21-hydroxylase defect. In the present series, the enzymatic defect was found to have a considerably lower prevalence than in a previous study of smaller size (15% vs 66%); however, considering the low frequency of the gene coding for the defect in the general population (0.015-0.057), the present results confirm an increased risk for non-classic 21-hydroxylase deficiency in HLA-B14 positive individuals. Therefore, in these subjects, a screening for 21-hydroxylase deficiency may be indicated.

摘要

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