Classical and non-classical congenital adrenal hyperplasia: What is the difference in subsequent fertility?

被引:0
|
作者
Carriere, Camille [1 ,2 ]
Sarfati, Cynthia [1 ,2 ,3 ]
Tejedor, Isabelle [1 ,2 ]
Dulon, Jerome [1 ,2 ]
Chakhtoura, Zeina [1 ,2 ]
Courtillot, Carine [1 ,2 ]
Bachelot, Anne [1 ,2 ,3 ]
机构
[1] Hop La Pitie Salpetriere, AP HP, IE3M, Dept Endocrinol & Reprod Med, Paris, France
[2] ICAN, Ctr Reference Pathol Gynecol Rares, Ctr Reference Malad Endocriniennes Rares Croissan, Paris, France
[3] Sorbonne Univ, Paris, France
关键词
Congenital adrenal hyperplasia; 21 hydroxylase deficiency; Fertility; Pregnancy; REST TUMORS; 21-HYDROXYLASE DEFICIENCY; ADULT MALES; WOMEN; OUTCOMES; MEN; PREGNANCY; COHORT; PREVALENCE; ADOLESCENT;
D O I
10.1016/j.o.2022.04.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
21-Hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal hyperplasia. Increased production of adrenal-derived androgens and progesterone in 21OHD women interfere with their reproductive function and their fertility in many different ways, depending on the severity of the disease. Sexuality and fertility in women with classic 21OHD is impaired, due to several issues such as disrupted gonadotropic axis due to androgen and progesterone overproduction, and mechanical, psychological factors related to genital surgery. Fertility and fecundity in these women get better over the years. Subfertility seems contrariwise to be relative in non-classic 21OHD women. Before pregnancy, genotyping the partner and genetic counselling is mandatory. (c) 2022 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:181 / 185
页数:5
相关论文
共 50 条
  • [31] Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia
    Isik, Recep Oguzhan
    Kizilcan Cetin, Sirmen
    Cetinkaya, Semra
    Berberoglu, Merih
    Siklar, Zeynep
    Ozsu, Elif
    Aycan, Zehra
    CLINICAL ENDOCRINOLOGY, 2023, 99 (02) : 135 - 141
  • [32] Two cases of male patients followed for a classical form of congenital adrenal hyperplasia (CAH), presenting an azoospermia: analysis and review of the literature
    Fouques, Cielia
    Fatfouta, Imene
    Hieronimus, Sylvie
    Sadoul, Jean-Louis
    Bongain, Andre
    BASIC AND CLINICAL ANDROLOGY, 2019, 29 (1)
  • [33] Non-classic congenital adrenal hyperplasia
    Witchel, Selma Feldman
    STEROIDS, 2013, 78 (08) : 747 - 750
  • [34] Fertility in patients with congenital adrenal hyperplasia
    Claahsen-van der Grinten, H. L.
    Stikkelbroeck, N. M. M. L.
    Sweep, C. G. J.
    Hermus, A. R. M. M.
    Otten, B. J.
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2006, 19 (05) : 677 - 685
  • [35] Anthropometric and Pubertal Outcomes in Girls With Classical Congenital Adrenal Hyperplasia
    Kaur, Japleen
    Singla, Mandeep
    Bhansali, Anil
    Bhadada, Sanjay
    Walia, Rama
    INDIAN PEDIATRICS, 2022, 59 (07) : 535 - 538
  • [36] Absence of Testicular Adrenal Rest Tumors in Newborns, Infants, and Toddlers with Classical Congenital Adrenal Hyperplasia
    Kim, Mimi S.
    Koppin, Christina M.
    Mohan, Pankhuri
    Goodarzian, Fariba
    Ross, Heather M.
    Geffner, Mitchell E.
    De Filippo, Roger
    Kokorowski, Paul
    HORMONE RESEARCH IN PAEDIATRICS, 2020, 92 (03): : 157 - 161
  • [37] A Normal Baby Girl Born to a Chinese Woman with Classical Congenital Adrenal Hyperplasia
    Belaramani, K. M.
    Wong, L. M.
    Kwong, N. S.
    HONG KONG JOURNAL OF PAEDIATRICS, 2010, 15 (03) : 230 - 233
  • [38] Cosegregation of a novel homozygous CYP11B1 mutation with the phenotype of non-classical congenital adrenal hyperplasia in a consanguineous family
    Peters, C. J.
    Nugent, T.
    Perry, L. A.
    Davies, K.
    Morel, Y.
    Drake, W. M.
    Savage, M. O.
    Johnston, L. B.
    HORMONE RESEARCH, 2007, 67 (04) : 189 - 193
  • [39] Adrenal rest tissue in gonads of patients with classical congenital adrenal hyperplasia: Multicenter study of 45 French male patients
    Pierre, Peggy
    Despert, Francois
    Tranquart, Francois
    Coutant, Regis
    Tardy, Veronique
    Kerlan, Veronique
    Sonnet, Emmanuel
    Baron, Sabine
    Lorcy, Yannick
    Emy, Philippe
    Delavierre, Dominique
    Monceaux, Francoise
    Morel, Yves
    Lecomte, Pierre
    ANNALES D ENDOCRINOLOGIE, 2012, 73 (06) : 515 - 522
  • [40] Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OHD) in adult males: Clinical presentation, hormone function and the detection of adrenal and testicular adrenal rest tumors (TARTs)
    San Martin, Patricia
    Eugenio Russmann, Maria Laura
    Mendeluk, Gabriela
    Fabiana Fierro, Maria
    Marino, Roxana
    Pardes, Ester
    ENDOCRINOLOGIA DIABETES Y NUTRICION, 2021, 68 (04): : 227 - 235