Category:MELAS syndrome

From Wikimedia Commons, the free media repository
Jump to navigation Jump to search
<nowiki>miopatia mitocondriale con encefalopatia, acidosi lattica ed episodi tipo ictus; syndrome MELAS; Синдром MELAS; MELAS; نشانگان ملاس; MELAS症候群; MELAS sindromas; MELAS sendromu; MELAS; melas; Zespół MELAS; Syndroma MELAS; síndrome MELAS; Mitokondriosairaus; MELAS syndrome; متلازمة ميلاس; MELAS; MELAS; citopatia con miopatia del mitocondrio, di cui fa parte anche la sindrome MERRF, e l'atrofia ottica di Leber; maladie mitochondriale qui débute typiquement dans l'enfance se manifestant essentiellement par un syndrome neurologique; mitokondriell sjukdom; genetycznie uwarunkowana choroba mitochondrialna; хвороба; Krankheit; one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy; مرض يصيب الإنسان; mitochondriální onemocnění; MELAS; ミトコンドリア脳筋症・乳酸アシドーシス・脳卒中様発作症候群; MELAS; mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes; MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes; Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes; MELAS; Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke; MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS; Melas Syndrome; MELAS; MELAS-syndrom; MELAS-syndromet; melas-syndrom; melas-syndromet; MELAS; mitochondriální encefalopatie s laktátovou acidózou a stroke-like epizodami; Sindrome MELAS; encefalomiopatía mitocondrial, acidosis láctica y episodios parecidos a un accidente cerebrovascular; MELAS</nowiki>
MELAS syndrome 
one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy
Двусторонняя кальцификация базальных ганглев, легкая атрофия мозжечка, ишемические изменения, повышение лактата. Abu-Amero et al., 2009[1]
Upload media
Instance of
Subclass of
  • mitochondrial encephalomyopathy
  • neurometabolic disease
  • syndromic genetic deafness
  • mitochondrial disease with eye involvement
  • mitochondrial disease with hypertrophic cardiomyopathy
  • mitochondrial disease with dilated cardiomyopathy
  • syndrome associated with hypertrophic cardiomyopathy
  • mitochondrial disease with epilepsy
  • mitochondrial disease with peripheral neuropathy
  • mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA
Authority file
Edit infobox data on Wikidata

Subcategories

This category has the following 3 subcategories, out of 3 total.