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L-carnitina e deficit sistemico di carnitina Il deficit sistemico di carnitina una rara sindrome genetica autosomica recessiva, caratterizzata da un quadro clinico grave e progressivo contraddistinto da cardiomiopatia, miopatia scheletrica, ipoglicemia ed iperammonemia

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In the proximal small intestine, luminal absorption of low Ca 2+ concentrations involve mainly the transcellular route (vitamin D-dependent) and for high concentrations, the paracellular passive route (vitamin D-independent) is the predominant source for calcium absorption