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Acute encephalopathy of the temporal lobes leading to m.3243A & gt;G. When MELAS is not always MELAS
Publication date: Available online 21 July 2016 Source:Mitochondrion Author(s): Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, Vincenzo Montano, Annalisa LoGerfo, Gabriele Siciliano, Ubaldo Bonuccelli, Michelangelo Mancuso MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes) is a rare genetic condition whose differential diagnosis is often posed with juvenile stroke, but more rarely even with inflammatory/infectious encephalitis, causing diagnostic challenges. Here we report the case of a young man harbouring the m.3243A>G MELAS mutation presenting an ac...
Source: Mitochondrion - July 30, 2016 Category: Biochemistry Source Type: research

Acute encephalopathy of the temporal lobes leading to m3243A & gt;G. When MELAS is not always MELAS
Publication date: Available online 21 July 2016 Source:Mitochondrion Author(s): Elena Caldarazzo Ienco, Daniele Orsucci, Costanza Simoncini, Vincenzo Montano, Annalisa LoGerfo, Gabriele Siciliano, Ubaldo Bonuccelli, Michelangelo Mancuso MELAS syndrome (mitochondrial encephalopathy with lactic acidosis and stroke-like episodes) is a rare genetic condition whose differential diagnosis is often posed with juvenile stroke, but more rarely even with inflammatory/infectious encephalitis, causing diagnostic challenges. Here we report the case of a young man harbouring the m.3243A>G MELAS mutation presenting an ac...
Source: Mitochondrion - July 22, 2016 Category: Biochemistry Source Type: research