Arginase deficiency presenting with cerebral oedema and failure to thrive

Journal of Inherited Metabolic Disease

Volumn 23, Issue 5, 2000, Pages 517-518

  Harrington, J W ^a   Stiefel, M ^a   Gianos, E ^a  

^a WESTCHESTER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; ARGINASE; ARGININE; BENZOIC ACID;

AMINO ACID BLOOD LEVEL; ARTICLE; BRAIN EDEMA; CASE REPORT; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DIET THERAPY; DISEASE ASSOCIATION; ENZYME DEFICIENCY; FAILURE TO THRIVE; FEMALE; HUMAN; HYPERAMMONEMIA; INFANT; MENTAL DISEASE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PROTEIN RESTRICTION; URINALYSIS;

ARGINASE; BRAIN EDEMA; FAILURE TO THRIVE; FEMALE; HUMANS; HYPERARGININEMIA; INFANT; SODIUM BENZOATE;

EID: 0033916069     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005624616905     Document Type: Article

References (3)

1. Argininemia: A treatable genetic cause of spastic diplegia simulating cerebral palsy: Case reports and literature review
2. Argininimia treated from birth
3. Inborn errors of metabolism