Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood.

Rocchiccioli, F; Wanders, R J; Aubourg, P; Vianey-Liaud, C; Ijlst, L; Fabre, M; Cartier, N; Bougneres, P F

Rocchiccioli, F; Wanders, R J; Aubourg, P; Vianey-Liaud, C; Ijlst, L; Fabre, M; Cartier, N; Bougneres, P F.

Affiliation

Rocchiccioli F; Unité 188 INSERM, Saint Vincent de Paul Hospital, Paris, France.

Pediatr Res ; 28(6): 657-62, 1990 Dec.

Article in En | MEDLINE | ID: mdl-2284166

Subject(s)

Acyl-CoA Dehydrogenase, Long-Chain/deficiency; Cardiomyopathies/etiology; Muscular Diseases/etiology; Cardiomyopathies/metabolism; Female; Humans; Hypoglycemia/etiology; Hypoglycemia/metabolism; Infant; Lipid Metabolism; Liver/ultrastructure; Muscles/ultrastructure; Muscular Diseases/metabolism; Muscular Diseases/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Acyl-CoA Dehydrogenase, Long-Chain / Muscular Diseases / Cardiomyopathies Type of study: Etiology_studies / Prognostic_studies Limits: Female / Humans / Infant Language: En Journal: Pediatr Res Year: 1990 Document type: Article Affiliation country: France

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