了解唐氏综合征的遗传机制和认知障碍:走向整体方法

Yara Abukhaled1, Kenana Hatab1, Mohammad Awadhalla1

  • 1Department of Physiology and Immunology, College of Medicine, and Health Sciences, Khalifa University, 127788, Abu Dhabi, United Arab Emirates.

Journal of neurology
|August 10, 2023
PubMed
概括

唐氏综合症 (DS),是由人类染色体21 (HC21) 的额外副本引起的,是智力障碍 (ID) 的最常见的遗传原因. 本综述探讨了与DS相关的ID机制以及改善生活质量的潜在疗法.

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