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Pacing Clin Electrophysiol ; 27(5): 675-6, 2004 May.
Article in English | MEDLINE | ID: mdl-15125729

ABSTRACT

This case report describes ventricular fibrillation without overt cardiomyopathy as the presenting symptom of primary carnitine deficiency due to organic cation transporter 2 (OCTN2)-deficiency in a 15-year-old girl. Normally this disease presents early in life with hypoketotic hypoglycemia, muscle weakness, and/or cardiomyopathy. The patient fully recovered after carnitine supplementation. Recognition of this disease is important because its treatment is easy and effective.


Subject(s)
Carnitine/deficiency , Carnitine/therapeutic use , Membrane Proteins/deficiency , Organic Cation Transport Proteins , Ventricular Fibrillation/etiology , Adolescent , Carrier Proteins , Consanguinity , Female , Humans , Solute Carrier Family 22 Member 5
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