Can Boys Have Turner Syndrome? More than a Question of Semantics.

IF 2.4 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Sexual Development Pub Date : 2022-01-01 Epub Date: 2021-08-10 DOI:10.1159/000518092
Michelle M Knoll, Julie Strickland, Jill D Jacobson
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引用次数: 0

Abstract

Individuals with 45,X mosaicism with Y chromosome material raised as boys are not diagnosed with Turner syndrome, a label restricted to phenotypic females. We sought to determine if boys with 45,X mosaicism had features consistent with Turner syndrome. Twenty-two patients (14 girls, 8 boys) seen in our Differences of Sex Development (DSD) clinic were identified for review. Standardized height (z-scores) by sex of rearing and results of cardiology, renal, audiology, thyroid, and celiac screenings were recorded. All subjects had heights below the mean for sex. Z-scores were not significantly different between boys and girls (p = 0.185). There were no significant differences in the incidence of cardiac anomalies between boys and girls (p = 0.08). Girls were more likely to have additional screenings (p = 0.042), but there were no significant differences in the number of positive screenings between boys and girls (p = 0.332). Patients with 45,X mosaicism raised as boys appear to have features similar to patients with the same karyotype raised as girls. Routine screening of boys following the Turner Syndrome Clinical Practice Guidelines may allow early recognition of comorbidities. Additionally, obtaining karyotypes on boys with short stature or other features of Turner syndrome may identify unrecognized cases of 45,X mosaicism.

男孩会得特纳综合症吗?不仅仅是语义学的问题。
具有45,x嵌合性和Y染色体物质的个体作为男孩长大,不会被诊断为特纳综合征,这一标签仅限于表现型的女性。我们试图确定患有45x嵌合的男孩是否具有与特纳综合征一致的特征。22例患者(14名女孩,8名男孩)在我们的性别发育差异(DSD)诊所被确定为审查。记录按饲养性别划分的标准化身高(z分数)以及心脏病、肾脏、听力学、甲状腺和乳糜泻筛查结果。所有受试者的身高都低于性生活的平均值。男女学生z -score差异无统计学意义(p = 0.185)。男孩和女孩的心脏异常发生率无显著差异(p = 0.08)。女孩更有可能进行额外的筛查(p = 0.042),但男孩和女孩之间阳性筛查的数量没有显著差异(p = 0.332)。作为男孩长大的45x嵌合体患者似乎与作为女孩长大的相同核型患者具有相似的特征。按照特纳综合征临床实践指南对男孩进行常规筛查,可以早期发现合并症。此外,获得身材矮小或具有特纳综合征其他特征的男孩的核型可以识别未被识别的45,x嵌合体病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sexual Development
Sexual Development 生物-发育生物学
CiteScore
4.00
自引率
4.30%
发文量
25
审稿时长
>12 weeks
期刊介绍: Recent discoveries in experimental and clinical research have led to impressive advances in our knowledge of the genetic and environmental mechanisms governing sex determination and differentiation, their evolution as well as the mutations or endocrine and metabolic abnormalities that interfere with normal gonadal development. ‘Sexual Development’ provides a unique forum for this rapidly expanding field. Its broad scope covers all aspects of genetics, molecular biology, embryology, endocrinology, evolution and pathology of sex determination and differentiation in humans and animals. It publishes high-quality original research manuscripts, review articles, short reports, case reports and commentaries. An internationally renowned and multidisciplinary editorial team of three chief editors, ten prominent scientists serving as section editors, and a distinguished panel of editorial board members ensures fast and author-friendly editorial processing and peer reviewing.
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