相关实验视频
Updated: May 10, 2025

Robotic Myotomy and Partial Fundoplication for Achalasia
Published on: August 11, 2023
三重A综合症-一种罕见的遗传性阿哈拉西亚病因
Shivangini Duggal1, Monica Botros1, Emerald Zaw2
1Department of Internal Medicine, Texas Tech University Health Sciences Center, El Paso, TX.
三重A综合征 (TAS) 是一种罕见的遗传性疾病,由于AAAS基因突变,导致水症,头症和上腺功能不充分. 早期诊断和TAS的管理对于患者的结果至关重要.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 罕见疾病 罕见疾病
背景情况:
- 三重A综合征 (TAS) 是一种罕见的自体相衰退性疾病.
- 它的特征是赤症,赤症和上腺功能不充分.
- 由AAAS基因突变引起,影响ALADIN蛋白功能.
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