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Erschienen in: The Journal of Obstetrics and Gynecology of India 1/2012

01.12.2012 | Case Report

A Success Story in Congenital Adrenal Hyperplasia

Erschienen in: The Journal of Obstetrics and Gynecology of India | Sonderheft 1/2012

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Abstract

Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders characterized by enzyme defects in adrenal steroidogenic pathways. CAH due to 21-hydroxylase deficiency accounts for 95 % of cases. This case was diagnosed to have simple virilizing type of CAH and started on dexamethasone, and underwent genitoplasty and clitoroplasty at 25 years of age, then was married 3 years after surgery and conceived spontaneously 2 years after marriage, to deliver a healthy male baby. Thus, proper diagnosis and treatment with steroids and genitoplasty can give females with CAH a normal sexual, normal menstrual, and reproductive function.
Literatur
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Zurück zum Zitat Merke DeborahP. Approach to the adult with congenital adrenal hyperplasia due to 21-Hydroxylase deficiency. J Clin Endocrinol Metab. 2008;93(3):653–60.CrossRefPubMed Merke DeborahP. Approach to the adult with congenital adrenal hyperplasia due to 21-Hydroxylase deficiency. J Clin Endocrinol Metab. 2008;93(3):653–60.CrossRefPubMed
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Zurück zum Zitat Hagenfeldt K, Janson PO, Holmdahl G, et al. Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Reprod. 2008;23(7):1607–13.CrossRefPubMed Hagenfeldt K, Janson PO, Holmdahl G, et al. Fertility and pregnancy outcome in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Hum Reprod. 2008;23(7):1607–13.CrossRefPubMed
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Metadaten
Titel
A Success Story in Congenital Adrenal Hyperplasia
Publikationsdatum
01.12.2012
Erschienen in
The Journal of Obstetrics and Gynecology of India / Ausgabe Sonderheft 1/2012
Print ISSN: 0971-9202
Elektronische ISSN: 0975-6434
DOI
https://doi.org/10.1007/s13224-013-0387-1

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