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特纳综合征:一生面临的四大挑战。

Turner syndrome: four challenges across the lifespan.

作者信息

Sutton Erica J, McInerney-Leo Aideen, Bondy Carolyn A, Gollust Sarah E, King Donnice, Biesecker Barbara

机构信息

National Human Genome Research Institute, NIH, Bethesda, Maryland 20892-1852, USA.

出版信息

Am J Med Genet A. 2005 Dec 1;139A(2):57-66. doi: 10.1002/ajmg.a.30911.

Abstract

Turner syndrome (TS) is a sex chromosome condition that occurs in approximately 1/2,500 live female births. Despite the prevalence of this chromosomal condition, the challenges these women face throughout their lives are not fully understood. This qualitative research study aimed to characterize the subjective experiences of individuals with TS throughout their lifespan, to investigate their concerns and obstacles, and to offer insight into the strengths and weaknesses of health care delivery, as they perceived them. Ninety-seven girls and women with TS and 21 parents consented to participate in this interview study. Interviews were semi-structured and open-ended in design. Questions sought to elicit responses relating to existing concerns associated with their condition and positive and negative health care experiences. Participants were divided into four age categories (childhood, adolescence, adulthood, and mature adulthood) to facilitate a comparative analysis across the age spectrum. Regardless of age, infertility was the most frequently cited concern followed closely by short stature. Sexual development and function and general health were also viewed as challenges by a number of participants in each age group. Although the relative weight of these four concerns tended to shift based upon the individual's age and life experiences, all four issues remained significant throughout the lifespan. Enhanced awareness of the evolving physical and psychological challenges faced by girls and women with TS may help health care providers (HCPs) improve the quality of life for these individuals.

摘要

特纳综合征(TS)是一种性染色体疾病,约每2500例活产女婴中就有1例患病。尽管这种染色体疾病较为常见,但这些女性一生所面临的挑战尚未完全明晰。这项定性研究旨在描述特纳综合征患者一生的主观经历,调查她们所关心的问题和障碍,并深入了解她们所认为的医疗保健服务的优缺点。97名患有特纳综合征的女孩和女性以及21名家长同意参与这项访谈研究。访谈采用半结构化和开放式设计。问题旨在引出与她们病情相关的现存担忧以及积极和消极的医疗保健经历。参与者被分为四个年龄组(儿童期、青春期、成年期和成熟成年期),以便于进行全年龄范围的比较分析。无论年龄大小,不孕是最常被提及的担忧,紧随其后的是身材矮小。性发育与功能以及总体健康在每个年龄组的许多参与者眼中也被视为挑战。尽管这四个担忧的相对重要性往往会因个体年龄和生活经历而有所变化,但这四个问题在整个生命周期中都很重要。提高对患有特纳综合征的女孩和女性所面临的不断变化的身体和心理挑战的认识,可能有助于医疗保健提供者(HCPs)提高这些个体的生活质量。

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