MELAS syndrome - Wikipedia
网页MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes) is one of the family of mitochondrial diseases, which also include MIDD (maternally inherited diabetes and deafness), MERRF syndrome, and Leber's hereditary optic neuropathy. It was first characterized under this name in 1984. [2]
MELAS Syndrome: What It Is, Causes, Symptoms & Treatment - Cleveland Clinic
网页2023年7月24日 · MELAS syndrome is a mitochondrial disease that mostly affects your nervous system and muscles. It also causes lactic acid to collect in your body and may result in repeated events that are similar to strokes .
Melas Syndrome - StatPearls - NCBI Bookshelf
网页2024年1月25日 · Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome is a rare maternally inherited mitochondrial disorder that predominantly affects the nervous system and muscles. MELAS typically appears in childhood after a period of normal early development.
MELAS Syndrome - Symptoms, Causes, Treatment | NORD
网页2011年1月10日 · MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes) syndrome is a rare disorder that begins in childhood, usually between two and fifteen years of age, and mostly affects the nervous system and muscles.
Mitochondrial encephalomyopathy, lactic acidosis, and stroke …
网页2001年2月27日 · Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a condition that affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy). Explore symptoms, inheritance, genetics of this condition.
MELAS症候群 - 维基百科，自由的百科全书
网页粒線體異常引發之肌肉病變、腦病變、乳酸中毒、中風症候群 [1] ( Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes，MELAS) 是一種粒線體疾病，于 1984 年提出。 [2] 这些粒線體疾病是完全从母系遗传的粒線體基因缺陷導致。 [3]
中国线粒体脑肌病伴高乳酸血症和卒中样发作的诊治专家共识 - 中 …
网页线粒体脑肌病伴高乳酸血症和卒中样发作（mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes，MELAS）是一种由线粒体DNA（mitochondrial DNA，mtDNA）或核DNA（nuclear DNA，nDNA）突变导致的多系统代谢性疾病 [1, 2]，以卒中样发作、癫痫发作、认知与精神障碍、高 ...
MELAS症候群 - 维基百科，自由的百科全书
网页2022年5月15日 · 线粒体异常引发之肌肉病变、脑病变、乳酸中毒、中风症候群[1] ( Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes， MELAS ) 是一种线粒体疾病，于 1984 年提出。 [2] 这些线粒体疾病是完全从母系遗传的线粒体基因缺陷导致。 [3] 病征和症状. [编辑] MELAS症候群可影响身体许多系统，尤其是神经与肌肉系统。 大多数病人在儿童期就发病。 病童的早期精神运动发展一般是正常的，但在 2 至 10 岁之间出 …
MELAS | About the Disease | GARD - Genetic and Rare Diseases ...
网页Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) affects many parts of the body, particularly the brain and nervous system (encephalo-) and muscles (myopathy). Symptoms typically begin in childhood and may include muscle weakness and pain, recurrent headaches, loss of appetite, vomiting, and seizures.
线粒体脑肌病伴乳酸酸中毒和卒中样发作 - 百度百科
网页线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）是以脑病、脑卒中样发作、乳酸血症为主要症状的线粒体病，是线粒体病中最常见的类型之一。. 患者可以有母系遗传的家族史，散发性患者也不少见。. 发病年龄从婴儿到成人期，以儿童期和青少年期发病居多 ...
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