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Updated: Jul 15, 2025

Quantification of Coenzyme A in Cells and Tissues
Published on: September 27, 2019
[苏西尼尔CoA:3氧酸CoA转移酶缺陷:一个病例报告]
Miguel Angel Jurado-Aguirre1, Ana Elena Pérez-Verdín1
1Instituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades "Lic. Ignacio García Téllez", Departamento de Endocrinología. Guadalajara, Jalisco, México.
糖CoA:3-氧酸CoA转移酶缺乏症 (SCOTD) 是一种罕见的代谢障碍. 早期诊断和治疗至关重要,特别是当高血糖症呈现异常时,以改善患者的治疗结果.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 苏奇尼尔-CoA:3-oxoacid CoA转移酶缺乏症 (SCOTD) 是一种罕见的自体逆向代谢障碍.
- 具有体利用能力受损的特征,导致急性酸性脂肪酸症发作.
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