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Clinical Features and Gene Mutations of 6 Patients with Carnitine Palmitoyltransferase 1A Deficiency

The most severe cause methylmalonic acidemia, a rare but life-threatening disorder that typically presents in infancy

Selection criteria Eligible trials were randomised controlled trials (RCTs) or quasiRCTs, parallelgroup or crossover, that compared Lcarnitine or its derivatives, acetylLcarnitine or propionylLcarnitine, at any dose and for any length of treatment, with placebo or no treatment in cognitively healthy people of any age and either gender

Mas deve-se estar atento ao fornecedor, especialmente quanto autenticidade e armazenamento da substncia

doi: 10.4103/1817-1745.193363

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