46,XX睾丸性发育差异的早期诊断:异常表现伴核半透明增加。

IF 0.7 4区 医学 Q4 PATHOLOGY Fetal and Pediatric Pathology Pub Date : 2024-03-01 Epub Date: 2023-10-30 DOI:10.1080/15513815.2023.2274831
Miguel Saraiva, Vera M F Santos, Lina Ramos, Fabiana Ramos, Joana Serra-Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante
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引用次数: 0

摘要

引言:46,XX睾丸性发育障碍(DSD)可能在产前表现为表型和核型之间的不匹配。颈部半透明增大是许多疾病的一个异常体征。我们报告了一个妊娠早期胎儿,其颈部半透明性增加,后来被确定为46,XX睾丸DSD。病例介绍:妊娠早期超声显示颈部半透明性增大。绒毛取样记录了一个46,XX染色体组型。随后的超声波检查确认了男性的外生殖器。FISH分析记录了SRY基因易位。婴儿出生时有正常的男性内外生殖器。结论:46,XX睾丸DSD可能在妊娠早期出现,并伴有颈部半透明增大。
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Early Diagnosis of 46,XX Testicular Difference of Sexual Development: Unusual Presentation with Increased Nuchal Translucency.

Introduction: 46,XX testicular disorder of sexual development (DSD) may present prenatally as a mismatch between phenotype and karyotype. Enlarged nuchal translucency is an abnormal sign of many disorders. We present a first trimester fetus with increased nuchal translucency that was later determined to be a 46,XX testicular DSD.

Case presentation: A first-trimester pregnancy ultrasound revealed enlarged nuchal translucency. Chorionic villous sampling documented a 46,XX karyotype. Subsequent ultrasounds identified male external genitalia. FISH analysis documented a SRY gene translocation. At birth, the infant had normal male internal and external genitalia.

Conclusions: 46,XX testicular DSD may present in the first trimester with an enlarged nuchal translucency.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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