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Last Updated: June 3, 2026 Introduction to Carnitine Deficiency, Systemic Primary (CDSP) Carnitine deficiencies lead to an inability to transport long-chain fatty acids (as fatty acylcarnitines) into the mitochondria for oxidation

D.Martnez-MedinaA.Ortiz-CominoC.Balaguer-Bernaldo-de-QuirsC.et al

Carnitine and total parenteral nutrition of the neonate

Furthermore, under normal physiological conditions following birth, term newborns readily acquire sufficient L-carnitine through enteral feeds

L-carnitine, also known as L-b-hydroxy-g-N-trimethylaminobutyric acid, is a natural substance that plays a role in the transportation of fatty acids to the mitochondria for metabolism

Through comparison between digital biomarkers retrieved by these sensors and the MFIS (completed by the patients every 4 weeks), the burden of fatigue and its worsening through social isolation could be reported