Classic congenital adrenal hyperplasia: A delayed presentation | Siddiqui | Pakistan Journal of Medical Sciences
 

Classic congenital adrenal hyperplasia: A delayed presentation

Saima Aziz Siddiqui, Nargis Soomro, Ashraf Ganatra

Abstract


Congenital adrenal hyperplasia (CAH) is a rare congenital disorder, which in cases of female genotype may result in virilization. Specific enzyme deficiencies in adrenocorticoid hormones biosynthetic pathway lead to excess androgen production causing virilization. Classic type presents early in infant life as salt losing or simple virilizing type, whereas non classic form presents late at puberty or in adult life. Depending on the type of classic CAH, type of adrenocorticoid deficiency, extent of virilization & genotype, surgical corrective procedures, glucocorticoid & mineralocorticoid replacement therapy are the mainstay of management. We present here a case of classic congenital adrenal hyperplasia of simple virilizing type, which presented later in childhood.

doi: http://dx.doi.org/10.12669/pjms.291.2830

How to cite this:Siddiqui SA, Soomro N, Ganatra A. Classic congenital adrenal hyperplasia: A delayed presentation. Pak J Med Sci 2013;29(1):220-223.   doi: http://dx.doi.org/10.12669/pjms.291.2830

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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