儿童开始的亨廷顿病. 一个罕见的呈现形式
A Gauto1, E Bellantonio1, P Pedernera-Bradichansky1
1Hospital de Pediatría Juan P. Garrahan, CABA, Argentina.
Revista de neurologia
|February 28, 2024
概括
儿童发病的亨廷顿病 (HD) 呈现出独特的症状,如运动和发育迟缓,与成人形式不同. 早期识别至关重要,特别是与家族史,由于预期现象.
科学领域:
- 神经学 神经学
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
背景情况:
- 亨廷顿病 (HD) 是一种罕见的自体主导神经退行性疾病.
- 它是由亨廷丁基因的CAG三倍扩张引起的,导致预期 (在连续几代中更早发病).
- 儿童发病的HD (10岁之前) 与成年形式相比,呈现出不同的临床特征.
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