Recurrent rhabdomyolysis in a child with glutaric aciduria type I

Journal of Inherited Metabolic Disease

Volumn 22, Issue 5, 1999, Pages 663-664

  Wilson, C J ^a   Collins, J E ^a   Leonard, J V ^b  

^a GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTARIC ACID;

ACIDURIA; ARTICLE; CASE REPORT; CLINICAL FEATURE; HUMAN; MALE; RHABDOMYOLYSIS; SCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; FOLLOW-UP STUDIES; GLUTARATES; HUMANS; MALE; RECURRENCE; RHABDOMYOLYSIS;

EID: 0033028982     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005542400135     Document Type: Article

References (3)

1. Bertorini TE (1997) Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome. Neuro-Clin 15: 649-671.
2. Hoffman GF, Bohles HJ, Burlina A, et al (1995) Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency. J Inher Metab Dis 18: 173-176.
3. Superti-Furga A, Hoffman GF (1997) Glutaric aciduria type 1 (glutaryl-CoA-dehydrogenase): advances and unanswered questions. Eur J Pediatr 156: 821-828.