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Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Mitochondrial Encephalomyopathies > MELAS Syndrome
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Mitochondrial Encephalomyopathies > MELAS Syndrome
... > Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Mitochondrial Myopathies > Mitochondrial Encephalomyopathies > MELAS Syndrome
Musculoskeletal Diseases > Muscular Diseases > Mitochondrial Myopathies > Mitochondrial Encephalomyopathies > MELAS Syndrome
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Mitochondrial Diseases > Mitochondrial Myopathies > Mitochondrial Encephalomyopathies > MELAS Syndrome
Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > MELAS Syndrome
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > MELAS Syndrome
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > MELAS Syndrome
Cardiovascular Diseases > Vascular Diseases > Cerebrovascular Disorders > Cerebral Small Vessel Diseases > MELAS Syndrome
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Cerebrovascular Disorders > Cerebral Small Vessel Diseases > MELAS Syndrome

Preferred term

MELAS Syndrome  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • MELAS
  • Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
  • Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
  • Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
  • Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke

Scope note

  • A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)

History note

  • 1993

In other languages

URI

http://www.yso.fi/onto/mesh/D017241

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