URINARY EXCRETION OF 17-KETOSTEROIDS IN VARIOUS CONDITIONS OF OLIGOPHRENIA CORRELATED WITH SOME AUTOPSY OBSERVATIONS
- 1 July 1947
- journal article
- research article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 7 (7) , 503-518
- https://doi.org/10.1210/jcem-7-7-503
Abstract
Twenty-four hr. urinary excretion of 17-ketosteroids was studied in several conditions of mental deficiency with and without endocrine disorders. Urinary 17-ketosteroid excretion was found normal for familial morons of both sexes, consistent with normal adrenocortical and gon-adal activity. Myotonia dystrophica was found to be associated with a marked decrease in urinary 17-ketosteroids, consistent with the pathology. Three cretins and an hypo-thyroid patient had low 17-ketosteroid excretion, in line with previous reports in the literature of low androgens in hypo-thyroidism. Findings for 9 mongoloid patients were in agreement with those for 23 cases reported earlier. Mongoloid children and [female] mongoloids had avg. to high, or low 17-ketosteroid excretion. Mongoloid [male][male] of adult age have a 17-ketosteroid excretion in the [female] range, consistent with their known sexual immaturity. Autopsy findings were considered in relation to the 17-ketosteroid excretion and the significance of these observations was discussed.This publication has 5 references indexed in Scilit:
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