线粒体3 - 基-3 - 甲基氨酸-辅酶A合成酶2缺乏症与儿童严重高血糖症:一个罕见的病例报告
Chang Dong1, Tiantian Lu1, Yazhou Jiang1
1Department of Pediatrics, The Affiliated Suqian Hospital of Xuzhou Medical University, China.
线粒体3 - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 甲基甲基甲酶A合成酶2 (HMGCS2) 缺乏,是一种罕见的代谢障碍,可以出现严重的高血糖症,而不仅仅是低血糖症. 这一案例突显出一种非典型的表现,有助于早期诊断.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
背景情况:
- 线粒体3 - 基-3 - 甲基酸 - 共酶A合成酶2 (HMGCS2) 缺乏症是一种罕见的自体逆向性疾病,影响生成.
- 通常在禁食或代谢压力期间呈现低血糖症.
- 严重的高血糖作为最初的症状是不寻常的.
研究的目的:
- 报告HMGCS2缺乏症的病例,呈现严重的高血糖症.
- 强调识别非典型的临床特征对于早期诊断的重要性.
主要方法:
- 一个六个月大的女孩在禁食后昏迷的案例报告.
- 临床和生化评估,包括血糖,和氨水平.
- 整体外基因组测序以识别HMGCS2基因突变.
主要成果:
- 该患者表现出严重的高血糖症 (25.8 mmol/L),尿,代谢性酸化,肝酶升高和高血糖.
- 遗传分析显示,HMGCS2基因 (c.1175C>T和c.719A>T) 中存在复合异构基因突变.
- 禁食胰岛素,葡萄糖和糖化血红蛋白水平正常.
结论:
- 严重的高血糖症可能是HMGCS2缺乏症的非典型表现特征.
- 提高对罕见症状的认识对于及时诊断和管理HMGCS2缺乏至关重要.
更多相关视频
09:40Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle
Published on: January 19, 2017
08:56Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
Published on: October 10, 2025
相关概念视频
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Diabetes Mellitus: Overview and Type I Subtype
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
Inborn Errors of Metabolism
Type I Diabetes III: Clinical Manifestations
Type II Diabetes Mellitus III: Clinical Manifestations and Diagnosis
Hyperglycemia
