Literature DB >> 27741188

Disorders of Sexual Development in Adult Women.

Veronica Gomez-Lobo1, Anne-Marie Amies Oelschlager.   

Abstract

Disorders (differences) of sexual development encompass a variety of conditions with atypical development of chromosomal, gonadal, or anatomic sex. Three of the most common differences of sex development conditions include congenital adrenal hyperplasia, complete androgen insensitivity, and Turner syndrome. Obstetrician-gynecologists who care for affected individuals in their practice must be familiar with the genetic, endocrine, and anatomic considerations of the most common conditions to provide optimal care. As women with these conditions transition to adult care, the gynecologist needs to assess the patient's understanding and educate her regarding her diagnosis and ongoing medical care. All of these conditions may affect self-perception, mental health, fertility, sexual function, and bone and cardiovascular health. Women with congenital adrenal hyperplasia need lifelong endocrine management and require genetic counseling before pregnancy. Women with androgen insensitivity syndrome require counseling regarding gonadectomy and hormone replacement therapy and may require vaginal elongation for intercourse. Most women with Turner syndrome experience premature ovarian insufficiency and require long-term estrogen replacement. Women with Turner syndrome often have congenital anomalies and autoimmune disorders, which require regular monitoring and care during adulthood. The purpose of this review is to provide the obstetrician-gynecologist who cares for adult women with the most common disorders (differences) of sexual development conditions an outline of the current recommendations for screening and ongoing health care with particular emphasis on the underlying genetics, management of subfertility, infertility and sexual concerns, approach to hypogonadism, and understanding of associated comorbidities.

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Mesh:

Year:  2016        PMID: 27741188      PMCID: PMC5119649          DOI: 10.1097/AOG.0000000000001672

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  64 in total

Review 1.  Gender dysphoria and gender change in chromosomal females with congenital adrenal hyperplasia.

Authors:  Arianne B Dessens; Froukje M E Slijper; Stenvert L S Drop
Journal:  Arch Sex Behav       Date:  2005-08

2.  Systemic hypotensive effects of testosterone are androgen structure-specific and neuronal nitric oxide synthase-dependent.

Authors:  Mercedes Perusquía; Clayton D Greenway; Lisa M Perkins; John N Stallone
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-05-06       Impact factor: 3.619

3.  Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene.

Authors:  D L S Danilovic; P H S Correa; E M F Costa; K F S Melo; B B Mendonca; I J P Arnhold
Journal:  Osteoporos Int       Date:  2006-11-01       Impact factor: 4.507

4.  Careful cardiovascular screening and follow-up of women with Turner syndrome before and during pregnancy is necessary to prevent maternal mortality.

Authors:  Celine Chalas Boissonnas; Celine Davy; Marie Bornes; Leila Arnaout; Christophe Meune; Vassilis Tsatsatris; Alexandre Mignon; Pierre Jouannet
Journal:  Fertil Steril       Date:  2008-11-06       Impact factor: 7.329

5.  Pregnancies in patients with congenital adrenal hyperplasia with complete or almost complete impairment of 21-hydroxylase activity.

Authors:  Wolfgang Hoepffner; Egbert Schulze; Joachim Bennek; Eberhard Keller; Helmut Willgerodt
Journal:  Fertil Steril       Date:  2004-05       Impact factor: 7.329

6.  Ascertainment bias in Turner syndrome: new insights from girls who were diagnosed incidentally in prenatal life.

Authors:  Daniel F Gunther; Erica Eugster; Anthony J Zagar; Constance G Bryant; Marsha L Davenport; Charmian A Quigley
Journal:  Pediatrics       Date:  2004-09       Impact factor: 7.124

7.  Tuberous breast: revised classification and a new hypothesis for its development.

Authors:  Michel Costagliola; Bishara Atiyeh; Florence Rampillon
Journal:  Aesthetic Plast Surg       Date:  2013-04-30       Impact factor: 2.326

8.  Spectrum of aortic valve abnormalities associated with aortic dilation across age groups in Turner syndrome.

Authors:  Laura J Olivieri; Ridhwan Y Baba; Andrew E Arai; W Patricia Bandettini; Douglas R Rosing; Vladimir Bakalov; Vandana Sachdev; Carolyn A Bondy
Journal:  Circ Cardiovasc Imaging       Date:  2013-10-01       Impact factor: 7.792

9.  Livebirth after uterus transplantation.

Authors:  Mats Brännström; Liza Johannesson; Hans Bokström; Niclas Kvarnström; Johan Mölne; Pernilla Dahm-Kähler; Anders Enskog; Milan Milenkovic; Jana Ekberg; Cesar Diaz-Garcia; Markus Gäbel; Ash Hanafy; Henrik Hagberg; Michael Olausson; Lars Nilsson
Journal:  Lancet       Date:  2014-10-06       Impact factor: 79.321

10.  Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia.

Authors:  Naomi S Crouch; Lih Mei Liao; Christopher R J Woodhouse; Gerard S Conway; Sarah M Creighton
Journal:  J Urol       Date:  2007-12-21       Impact factor: 7.450

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  4 in total

1.  46,XY Disorder of Sex Development Caused by 17α-Hydroxylase/17,20-Lyase Deficiency due to Homozygous Mutation of CYP17A1 Gene: Consequences of Late Diagnosis.

Authors:  Giampaolo Papi; Rosa Maria Paragliola; Paola Concolino; Carlo Di Donato; Alfredo Pontecorvi; Salvatore Maria Corsello
Journal:  Case Rep Endocrinol       Date:  2018-04-24

2.  Identification of a novel mutation in the SRD5A2 gene of one patient with 46,XY disorder of sex development.

Authors:  Shu-Ping Li; Li-Wei Li; Ming-Xia Sun; Xin-Xin Chen; Xiu-Feng Wang; Zeng-Kui Li; Sheng-Yun Zhou; Dong-Cai Zhai; Shu-Xia Geng; Shu-Jun Li; Xiao-Wei Dou
Journal:  Asian J Androl       Date:  2018 Sep-Oct       Impact factor: 3.285

3.  Isochromosome Mosaic Turner Syndrome: A Case Report.

Authors:  Mark Ramon Victor Llanes; May Uyking-Naranjo
Journal:  J ASEAN Fed Endocr Soc       Date:  2019-11-09

4.  Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development.

Authors:  Liwei Li; Junhong Zhang; Qing Li; Li Qiao; Pengcheng Li; Yi Cui; Shujun Li; Shirui Hao; Tongqian Wu; Lili Liu; Jianmin Yin; Pingsheng Hu; Xiaowei Dou; Shuping Li; Hui Yang
Journal:  Ital J Pediatr       Date:  2022-03-24       Impact factor: 2.638

  4 in total

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