Gastrointestinal complications of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome managed by parenteral nutrition

MELAS – an acronym for mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes – is a multiorgan disease caused by a mutation in mitochondrial DNA (mtDNA). Its clinical manifestations are highly variable; mainly stroke-like episodes, seizures, recurrent headaches, or muscle weaknes...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Simona Horná, Martin Jozef Péč, Juraj Krivuš, Renáta Michalová, Štefan Sivák, Peter Galajda, Marián Mokáň
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	SMC MEDIA SRL 2024-01-01
Σειρά:	European Journal of Case Reports in Internal Medicine
Θέματα:	melas nutrition superior mesenteric artery syndrome
Διαθέσιμο Online:	https://www.ejcrim.com/index.php/EJCRIM/article/view/4268
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