在兄弟姐妹之间BBS1的临床变异性
Vanna Giang1, Sarah R Weber2,3, Jeffrey M Sundstrom2,3
1Ophthalmology, Penn State College of Medicine, Hershey, Pennsylvania, USA vgiang@pennstatehealth.psu.edu.
BMJ case reports
|December 10, 2024
概括
巴德特-比德尔综合征 (BBS) 是一种罕见的遗传疾病. 这项研究强调了单基因变异 (BBS1) 如何在兄弟姐妹中引起不同的症状,从而使诊断复杂化.
科学领域:
- 遗传学 是一个遗传学.
- 纤维病变是一种纤维病变.
- 罕见疾病是一种罕见的疾病.
背景情况:
- 巴德特-比德尔综合征 (BBS) 是一种罕见的自体衰退性纤毛病,具有多种临床表现.
- 由于BBS的罕见性和显著的表型变异性,诊断具有挑战性.
- 多个基因与BBS有关,进一步使遗传诊断复杂化.
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