骨表型总是存在的,但在PAPSS2缺乏症中,雄激素过量较少见
Didem Helvacıoğlu1, Tülay Güran1
1Marmara University Faculty of Medicine, Department of Pediatric Endocrinology and Diabetes, İstanbul, Turkey
Journal of clinical research in pediatric endocrinology
|December 12, 2023
概括
3-adenosine 5-硫酸合成酶2 (PAPSS2) 缺乏症是一种罕见的遗传性疾病. 本综述总结了79名报告患者的临床,分子和生化特征,重点关注骨发育不良和雄激素过量.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 骨发育不良症 骨发育不良症
背景情况:
- 3-adenosine 5-硫酸合成酶2 (PAPSS2) 缺乏症是一种罕见的遗传性疾病.
- 由PAPSS2基因中的双性致病变体引起,首次描述于1998年.
- 以前在79名患者中报告过,其特点是骨异常和雄激素过量.
研究的目的:
- 审查和总结PAPSS2缺乏的临床,分子和生化特征.
- 巩固当前有关该疾病表现和遗传基础的知识.
- 为临床医生和研究人员提供全面的概述.
主要方法:
- 关于PAPSS2缺乏的已发表病例的文献综述.
- 临床发现的分析,包括骨和内分泌特征.
- 来自报告患者的分子和生化数据的汇编.
主要成果:
- 主要特征是不成比例的矮身和脊柱骨发育不良.
- 抗雄激素过量不太常见,但在临床上是显著的.
- 该综述整合了79名患者的数据,详细说明了他们的各种表现.
结论:
- PAPSS2 缺乏症主要表现为骨发育不良,较少出现雄激素过多.
- 了解这些特征对于准确的诊断和管理至关重要.
- 进一步的研究可能会阐明全谱和基因型-表型相关性.
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