Review and management of 46,XY Disorders of Sex Development

被引:30
|
作者
Massanyi, Eric Z. [1 ]
DiCarlo, Heather N. [1 ]
Migeon, Claude J. [2 ]
Gearhart, John P. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, James Buchanan Brady Urol Inst, Div Pediat Urol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Div Pediat Endocrinol, Baltimore, MD 21287 USA
关键词
46; XY Disorders of Sex Development; Androgen insensitivity syndrome; Gender assignment; Vaginoplasty; COMPLETE ANDROGEN INSENSITIVITY; AMBIGUOUS GENITALIA; GENDER-ASSIGNMENT; INITIAL MANAGEMENT; INTERSEX; DEFICIENCY; DIFFERENTIATION; INDIVIDUALS; HYPOSPADIAS; MUTATIONS;
D O I
10.1016/j.jpurol.2012.12.002
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Disorders of Sex Development (DSD) among 46,XY individuals are rare and challenging conditions. Abnormalities of karyotype, gonadal formation, androgen synthesis, and androgen action are responsible for the multiple disorders that result in undervirilization during development. Phenotypic appearance and timing of presentation are quite variable. The focus of treatment has shifted from early gender assignment and corrective surgery to careful diagnosis, proper education of patients and their families, and individualized treatment by a multi-disciplinary team. The modern management of these patients is difficult and controversial. Conflicting data on long-term outcomes of these individuals have been reported in the literature. The various etiologies of 46, XY DSD, current approaches to diagnosis and treatment, and reported long-term results are reviewed. (C) 2012 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:368 / 379
页数:12
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