Literature DB >> 20362972

Ovarian dysfunction by activating mutation of GS alpha: McCune-Albright syndrome as a model.

P Chanson1, S Salenave, J Young.   

Abstract

The McCune-Albright syndrome is characterized by cafe-au-lait spots, precocious puberty, and fibrous dysplasia. It is due to mutations in the gene encoding the GS protein alpha subunit coupling 7-transmembrane-domain receptors to adenylate cyclase, leading to constitutive adenylate cyclase activation and cAMP overproduction. Endocrinologists and gynecologists are confronted with new issues when these children reach adulthood. Gonadal function and fertility are often abnormal in women in whom puberty was precocious, owing to the persistence of a variable degree of ovarian autonomy that hinders adequate follicular development and ovulation. Copyright 2010. Published by Elsevier Masson SAS.

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Year:  2010        PMID: 20362972     DOI: 10.1016/j.ando.2010.02.015

Source DB:  PubMed          Journal:  Ann Endocrinol (Paris)        ISSN: 0003-4266            Impact factor:   2.478


  2 in total

1.  Characterization and management of testicular pathology in McCune-Albright syndrome.

Authors:  Alison M Boyce; William H Chong; Thomas H Shawker; Peter A Pinto; W Marsten Linehan; Nisan Bhattacharryya; Maria J Merino; Frederick R Singer; Michael T Collins
Journal:  J Clin Endocrinol Metab       Date:  2012-06-28       Impact factor: 5.958

2.  Treatment of primary infertility in McCune-Albright syndrome: a case report of a successful in vitro fertilization cycle.

Authors:  Rebecca K Chung; Abigail C Mancuso; Jessica D Kresowik
Journal:  F S Rep       Date:  2021-05-20
  2 in total

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