Ketogenic diet treatment of defects in the mitochondrial malate aspartate shuttle and pyruvate carrier

HIGHLIGHTS

• who: Bigna K. Bu00f6lsterli and collaborators from the Department of Pediatric Neurology, University Children`s Hospital Zurich, Zurich, Switzerland have published the research work: Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier, in the Journal: Nutrients 2022, 14, 3605. https:// of 15/08/2022
• what: MPC1 is expressed in many organs, and the authors here present the first individual with the additional features of splenomegaly, bone fractures after minor trauma and insulin-dependent, anti-body negative diabetes_mellitus. In MPC1-deficiency, the authors report for the first time a beneficial . . .
  

   

  

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