Literature DB >> 17727172

[Polycystic ovary syndrome and congenital adrenal hyperplasia: a different entity for comparable phenotypes?].

Damien Robyr1, Juan Llor, Georges Gaudin, Nicolas Schneider.   

Abstract

The phenotypes of the polycystic ovarian syndrome (PCOS) and congenital adrenal hyperplasia syndrome (CAHS) present a number of similarities. The main symptoms of PCOS are obesity, menstrual disorders, hirsutism, and low fertility in which the pituitary and adrenal glands are spared. The CAHS is a group of various entities all characterised by different degrees of malfunction of the 21-hydroxylase (CYP21) enzyme. The consequences are a downfall of the levels of aldosterone and cortisol, and the hyperproduction of adrenal androgen hormones. It is capital to be able to recognise these 2 entities in terms of identification of high risk families because the female foetuses suffering from CAHS will undergo severe virilization of there genitals in utero, which can efficiently be prevented by a administration of corticotherapy to the mother throughout the pregnancy.

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Year:  2007        PMID: 17727172

Source DB:  PubMed          Journal:  Rev Med Suisse        ISSN: 1660-9379


  2 in total

1.  17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses

Authors:  Seher Polat; Yusuf Kemal Arslan
Journal:  J Clin Res Pediatr Endocrinol       Date:  2021-11-08

Review 2.  Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency.

Authors:  Mouna Feki Mnif; Mahdi Kamoun; Faten Hadj Kacem; Fatma Mnif; Nadia Charfi; Basma Ben Naceur; Nabila Rekik; Mohamed Abid
Journal:  Indian J Endocrinol Metab       Date:  2013-09
  2 in total

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