在248名患有骨发育不良的印度人中,遗传和等位基因异质性
Prince Jacob1, Swati Singh1, Gandham SriLakshmi Bhavani1
1Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India.
European journal of human genetics : EJHG
|December 20, 2024
概括
这项研究使用基因组测试诊断了145个印度家庭的骨发育不良,在73个基因中确定了149种因果变异. 这些发现扩大了对亚洲印第安人罕见遗传骨疾病的理解.
科学领域:
- 遗传学 是一个遗传学.
- 罕见疾病 罕见疾病
- 骨生物学 骨生物学
背景情况:
- 骨发育不良是一种罕见的,遗传多样性的疾病.
- 大规模的队列研究对于了解疾病流行病学,表型和突变至关重要.
研究的目的:
- 在印度队伍中调查骨性失调的遗传基础和表型谱.
- 评估基因组测试在这些罕见疾病中的诊断产量.
主要方法:
- 197个骨发育不良的家庭的临床分子诊断.
- 向基因分析和下一代测序 (外基因组和基因组).
- 鉴定和鉴定因果变体和基因的特征.
主要成果:
- 实现了73.6%的诊断收益率 (145/197个家庭).
- 在73个基因中确定了149种因果变异 (85种新型),揭示了81种不同的单基因形式.
- 自体衰退形式占主导地位 (60%),血缘关系率高 (35%).
- 溶酶体储存疾病,与FGFR3相关的疾病和骨矿化障碍最常见.
结论:
- 基因组测试在临床和研究环境中有效诊断骨功能障碍.
- 这项研究扩大了骨失调的基因型和表型谱,包括新的基因疾病关系.
- 提供了关于骨发育不良频谱和亚洲印第安人的变体的关键数据.
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