剖析MAPT突变的临床异质性和基因型-表型相关性:一个系统性审查
Cristina Villa1, Elisa Pellencin1, Aurora Romeo1
1Neurology V and Neuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.
Frontiers in bioscience (Landmark edition)
|January 30, 2024
概括
微管相关蛋白 (MAPT) 基因的突变会导致遗传性前性痴呆症 (FTD),并带来各种症状. 虽然大多数MAPT突变表现出不同的临床特征,但有些与特定或混合的表型有关,使基因型-表型相关性复杂化.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 遗传学 是一个
- 神经学 神经学
背景情况:
- 微管相关蛋白 (MAPT) 突变是遗传前性痴呆症 (FTD) 的主要原因.
- FTD呈现出显著的临床异质性,通常表现为行为变体,但也更罕见的表型.
- 本综述综合了与MAPT突变相关的临床表型,以表征它们,并探索基因型-表型相关性.
结论:
- 与MAPT突变相关的FTD具有显著的临床异质性,具有有限的明显基因型-表型相关性.
- 某些表型特征可能会指导对MAPT突变的基因测试.
- 深入的患者表型和突变功能研究对于理解MAPT相关FTD临床变异性的生物学基础至关重要.
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