未诊断的罕见遗传疾病:变种功能性特征的重要性
1Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud Bin Abdulaziz University for Health Sciences, Riyadh 11426, Saudi Arabia.
Genes
|July 29, 2023
概括
罕见遗传性疾病 (RGD) 影响的人数不到2000人中的1人. 尽管这些疾病很罕见,但它们在全球范围内总共影响了超过3亿人,这突显了公共卫生面临的重大挑战.
科学领域:
- 遗传学 是一个遗传学.
- 公共卫生 公共卫生
- 医学研究 医学研究
背景情况:
- 罕见遗传性疾病 (RGD) 的定义在于它们的发病率很低,影响不到2000人中的1人.
- 总的来说,RGDs代表了相当大的全球健康负担,影响全球超过3亿人.
- 了解RGD的流行病学和影响对于制定有效的医疗保健策略至关重要.
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