16 三体综合征青少年内分泌异常:病例报告。

Fahad Naeem, Sohaib Sajid Zaheer, Khawaja Uzair, Mohsina Ibrahim
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引用次数: 0

摘要

染色体三体症的临床表现多种多样,从细微的症状到危及生命的情况都有,其中包括 16 三体综合征,它是头胎流产中最常见的非整倍体。大多数病例与产妇并发症和自然流产有关,通常在产前发现。患有 16 三体综合征而存活下来的婴儿通常会出现镶嵌变异,并可能表现出各种解剖和代谢异常,但 16 三体综合征的诊断并不保证一定会出现这些异常。我们分享了一个患有镶嵌型 16 三体综合征的 15 岁男孩的病例。他出生后即被确诊,症状轻微,没有任何重大的解剖学问题。然而,他确实出现了一些代谢问题,如胰岛素抵抗、肥胖、内分泌失调和维生素 D 缺乏。本报告重点介绍了 16 三体综合征的各种临床特征,并与之前报道的病例进行了比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endocrine Abnormalities in Mosaic Trisomy 16 Adolescent: A Case Report.

Chromosomal trisomy presents with a range of clinical manifestations, from subtle to life-threatening conditions that include trisomy 16, the most common aneuploidy in first trimester abortions. Most cases are linked to maternal complications and spontaneous abortions, typically detected prenatally. Infants who survive with trisomy 16 often have mosaic variants and may exhibit various anatomical and metabolic abnormalities, though a trisomy 16 diagnosis does not guarantee the presence of such abnormalities. We share the case of a 15-year-old boy who has mosaic trisomy 16. He was diagnosed after birth and showed mild symptoms without any major anatomical issues. However, he did experience several metabolic problems, such as insulin resistance, obesity, hormonal imbalances, and vitamin D deficiency. This report highlights the diverse clinical characteristics of trisomy 16, comparing them to previously reported cases.

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