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MELAS syndróm
Č. záznamu d017241 Dátum 06.06.2025 Typ M - MESH Tematický termín MELAS syndróm Iný termín Angličtina (Pseudonym) Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
Slovenčina (Pseudonym) myopatia mitochondriálna, encefalopatia, laktátová acidóza, epizódy podobné náhlej mozgovej príhode
Slovenčina (Pseudonym) encefalomyopatia mitochondriálna, laktoacidóza, epizódy podobné náhlej mozgovej príhode
MDT C05.651.460.620.520C10.228.140.163.100.535C10.228.140.300.275.500C10.668.491.500.500.500C14.907.253.329.500C16.320.565.189.535C18.452.132.100.535C18.452.648.189.535C18.452.660.560.620.520 Poznámka 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) 
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