Login / Signup

Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form.

Havva YazıcıGunes AkMerve Yoldas ÇelikFehime ErdemAyse Yuksel YanboluEsra ErAyse Ergul BozaciMerve Saka GüvençAyça AykutAsude Alpman DurmazEbru CandaSema Kalkan UçarMahmut Coker
Published in: Journal of pediatric endocrinology & metabolism : JPEM (2023)
Plasma acylcarnitine analysis should be preferred as it is superior to DBS acylcarnitine analysis in diagnosing CPT II deficiency. Even if plasma acylcarnitine analysis is impossible, CPT2 gene analysis should be performed. Our study emphasizes that CPT II deficiency should be considered in the differential diagnosis of recurrent rhabdomyolysis, even if typical acylcarnitine elevation does not accompany it.
Keyphrases
  • genome wide