Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey
Author(s) -
Claire Bouvattier,
Laure Esterle,
Peggy Renoult-Pierre,
Aude Brac de la Perrière,
F. Illouz,
V. Kerlan,
V. Pascal-Vigneron,
Delphine Drui,
Sophie Christin-Maître,
F. Galland,
Thierry Brue,
Yves Reznik,
F. Schillo,
D Pinsard,
X. Piguel,
G. Chabrier,
B. Decoudier,
Philippe Émy,
Igor Tauveron,
Marie-Laure Raffin-Sanson,
Jérôme Bertherat,
JeanMarc Kuhn,
Philippe Caron,
Maryse Cartigny,
Olivier Chabre,
Didier Dewailly,
Yves Morel,
Philippe Touraine,
Véronique Tardy-Guidollet,
Jacques Young
Publication year - 2015
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2014-4124
Subject(s) - azoospermia , medicine , endocrinology , population , congenital adrenal hyperplasia , pediatric endocrinology , infertility , pregnancy , biology , genetics , environmental health
Outcomes of congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency (21OHD) have been widely studied in children and women, but less so in men.
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