Very long-chain acyl-CoA dehydrogenase deficiency
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a condition that prevents the body from converting certain fats into energy, particularly during periods without food (fasting). …
VLCAD极长链酰基辅酶A脱氢酶缺乏症:引起低血糖、心肌病的脂肪 …
Very Long-Chain Acyl-CoA Dehydrogenase Deficiency 极长链酰基辅酶A脱氢酶缺乏症 （VLCADD）是一种罕见的脂肪酸代谢遗传性疾病，以常染色体隐性模式传播。 当分解某些 …
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
2009年5月28日 · Deficiency of very long-chain acyl-coenzyme A dehydrogenase (VLCAD), which catalyzes the initial step of mitochondrial beta-oxidation of long-chain fatty acids with a chain …
极长链酰基辅酶A脱氢酶缺乏症：症状与体征、病因、流行病学、 …
2022年8月27日 · 极长链酰基辅酶A脱氢酶缺乏症（VLCADD）是一种罕见的脂肪酸代谢遗传疾病，以常染色体隐性模式传播。 当分解某些非常长链脂肪酸所需的酶缺失或无法正常工作时， …
极长链酰基辅酶A脱氢酶缺乏症 - 百度百科
极长链酰基辅酶A脱氢酶（very long-chain acyl-CoA dehydrogenase，VLCAD）缺乏症是一种较罕见的遗传代谢病，由于线粒体内长链脂肪酸β氧化障碍导致能量代谢缺陷，为常染色体隐性遗 …
极长链酰基辅酶 A脱氢酶缺乏症筛诊治专家共识 - PMC
极长链酰基辅酶A脱氢酶（VLCAD）缺乏症是一种长链脂肪酸氧化代谢障碍性疾病，临床表现有明显异质性，新生儿到成年均可发病，以心脏、肝脏、骨骼肌及脑损害为主。 其中，心肌病型 …
Very long chain acyl-coa dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency (VLCAD deficiency) is a condition in which the body is unable to properly breakdown certain fats (called very long-chain fatty acids) into …
Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
2024年3月14日 · Learn about Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD), including symptoms, causes, and treatments. If you or a loved one is affected by this.
极长链酰基辅酶 A 脱氢酶（ACADVL）基因 - MCE-生物活性 ...
由该基因编码的蛋白质靶向线粒体内膜，在那里它催化线粒体脂肪酸 β-氧化途径的第一步。 这种酰基辅酶 A 脱氢酶对长链和超长链脂肪酸具有特异性。 该基因产物的缺乏会降低心肌脂肪酸β- …
Very long chain acyl-CoA dehydrogenase deficiency - Orphanet
Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is an inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: …