Adam Margaret P, Vilain Eric
Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington.
Departments of Human Genetics, Urology, and Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, California.
Am J Med Genet C Semin Med Genet. 2017 Jun;175(2):249-252. doi: 10.1002/ajmg.c.31564. Epub 2017 Jun 3.
Disorders/Differences of Sex Development (DSD), as defined by the 2006 Consensus Statement, are "congenital conditions in which development of chromosomal, gonadal, or anatomic sex is atypical." They represent a spectrum of chronic medical conditions collectively affecting about 1% of the population and are associated with increased risk of infertility, cancer, and psychosocial distress. Clinical management in DSD is subject to multiple controversies about gender assignment, the timing and appropriateness of genital surgery and the approach to disclosure. There is dissent within and between stakeholders (healthcare providers, advocacy groups, families) regarding what constitutes optimal care. This special issue investigates the progress made as well as the uncertainties remaining a decade after the consensus statement and the gaps to be filled by future research and improved clinical practice. It discusses the increasing intricacy of genetic variant interpretation in the era of next-generation sequencing and the associated complexity of phenotypic variability. The issue tackles ethical dilemmas and the complicated decision-making process of assignment of sex of rearing at birth in cases of 5-alpha reductase type 2 deficiency, surveys delivery of clinical services in the United States, discusses challenges of interdisciplinary care and of educating patients and parents about DSD,and reviews the factors predisposing to gonadal tumor and their consequences on clinical management.
性发育障碍/差异(DSD),根据2006年共识声明的定义,是“染色体、性腺或解剖学性别发育异常的先天性疾病”。它们代表了一系列慢性疾病,共同影响着约1%的人口,并与不孕、癌症和心理社会困扰风险增加有关。DSD的临床管理在性别指定、生殖器手术的时机和适当性以及信息披露方式等方面存在诸多争议。利益相关者(医疗保健提供者、倡导团体、家庭)内部和之间对于什么构成最佳护理存在分歧。本期特刊调查了自共识声明发布十年以来所取得的进展以及仍然存在的不确定性,以及未来研究和改进临床实践需要填补的空白。它讨论了在下一代测序时代基因变异解读日益增加的复杂性以及相关的表型变异性的复杂性。该特刊探讨了伦理困境以及在2型5-α还原酶缺乏症病例中出生时抚养性别的指定这一复杂的决策过程,调查了美国临床服务的提供情况,讨论了跨学科护理以及对患者和家长进行DSD教育的挑战,并回顾了性腺肿瘤的易感因素及其对临床管理的影响。