Literature DB >> 16835789

[Psychosexual aspects of intersex syndromes].

H A G Bosinski1.   

Abstract

Disorders of somatosexual development that lead to ambiguous genitalia occur in one from 3,000-5,000 newborns. Parents and health care professionals are confronted with a number of crucial questions: to what sex should the child be assigned, what is the appropriate treatment in terms of hormonal and surgical interventions, when and how should these take place, and what impact do they have on the development of gender identity (GI), psychosexual well-being and fertility? This paper reviews the etiology, treatment and outcome in terms of GI and sexual health for the following syndromes: congenital adrenal hyperplasia (CAH), complete and partial androgen insensitivity (cAIS, pAIS), and pure and mixed gonadal dysgenesis (pGD, mGD). Emphasis is focussed on the current discussion involving the timing and extent of genital surgery. Finally, a procedure is introduced that covers the sexual-medical needs of patients, parents and health care professionals.

Entities:  

Mesh:

Year:  2006        PMID: 16835789     DOI: 10.1007/s00120-006-1097-4

Source DB:  PubMed          Journal:  Urologe A        ISSN: 0340-2592            Impact factor:   0.639


  95 in total

1.  Gender self-reassignment in an XY adolescent female born with ambiguous genitalia.

Authors:  C Phornphutkul; A Fausto-Sterling; P A Gruppuso
Journal:  Pediatrics       Date:  2000-07       Impact factor: 7.124

2.  Managing intersex.

Authors:  S Creighton; C Minto
Journal:  BMJ       Date:  2001-12-01

3.  Anatomical studies of the fetal genitalia: surgical reconstructive implications.

Authors:  Laurence S Baskin
Journal:  Adv Exp Med Biol       Date:  2002       Impact factor: 2.622

4.  An examination of some basic sexual concepts: the evidence of human hermaphroditism.

Authors:  J MONEY; J G HAMPSON; J L HAMPSON
Journal:  Bull Johns Hopkins Hosp       Date:  1955-10

5.  Feminizing genitoplasty for congenital adrenal hyperplasia: what happens at puberty?

Authors:  N K Alizai; D F Thomas; R J Lilford; A G Batchelor; N Johnson
Journal:  J Urol       Date:  1999-05       Impact factor: 7.450

Review 6.  Molecular basis of androgen insensitivity.

Authors:  A O Brinkmann
Journal:  Mol Cell Endocrinol       Date:  2001-06-20       Impact factor: 4.102

7.  Behavioral effects of prenatal versus postnatal androgen excess in children with 21-hydroxylase-deficient congenital adrenal hyperplasia.

Authors:  S A Berenbaum; S C Duck; K Bryk
Journal:  J Clin Endocrinol Metab       Date:  2000-02       Impact factor: 5.958

8.  Behavioral and physical masculinization are related to genotype in girls with congenital adrenal hyperplasia.

Authors:  Catherine M Hall; Julie A Jones; Heino F L Meyer-Bahlburg; Curtis Dolezal; Michelle Coleman; Peter Foster; David A Price; Peter E Clayton
Journal:  J Clin Endocrinol Metab       Date:  2004-01       Impact factor: 5.958

9.  Genital surgery among females with congenital adrenal hyperplasia: changes over the past five decades.

Authors:  Peter A Lee; Selma F Witchel
Journal:  J Pediatr Endocrinol Metab       Date:  2002 Nov-Dec       Impact factor: 1.634

10.  A novel mutation in the D-box of the androgen receptor gene (S597R) in two unrelated individuals Is associated with both normal phenotype and severe PAIS.

Authors:  Yvonne L Giwercman; Sten A Ivarsson; Jonas Richthoff; Kristina B Lundin; Aleksander Giwercman
Journal:  Horm Res       Date:  2003-12-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.