CT‐scan Findings in an Infant with Glutaric Aciduria Type I

Developmental Medicine & Child Neurology

Volumn 30, Issue 6, 1988, Pages 808-811

  Yager, J Y ^a   McClarty, B M ^b   Seshia, S S ^c  

^a CHILDREN S HOSPITAL RESEARCH INSTITUTE OF MANITOBA   (Canada)

^b ST BONIFACE GENERAL HOSPITAL   (Canada)

^c UNIVERSITY OF MANITOBA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTARYL COENZYME A DEHYDROGENASE; RIBOFLAVIN;

ACIDURIA; AMINO ACID METABOLISM; CASE REPORT; CENTRAL NERVOUS SYSTEM; CLINICAL FEATURE; COMPUTER ANALYSIS; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSIS; FIBROBLAST CULTURE; HEREDITY; HUMAN; INFANT; MALE; METABOLIC DISORDER; PRIORITY JOURNAL; PROGNOSIS; PROTEIN RESTRICTION;

AMINO ACID METABOLISM, INBORN ERRORS; BRAIN; CASE REPORT; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; DISEASES IN TWINS; GENES, RECESSIVE; GLUTARATES; HUMAN; INFANT, NEWBORN; MALE; OXIDOREDUCTASES; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0024261514     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.1988.tb14643.x     Document Type: Article

References (12)

1. CT scans of infants with glutaric aciduria
2. Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features
3. Glutaric aciduria type I: biochemical investigations and post‐mortem findings
4. Treatment of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria)
5. Glutaric aciduria: biochemical and morphologic considerations
6. Hypothesis: a rôle for quinolinic acid in the neuropathology of glutaric aciduria type I
7. Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis
8. Intrauterine growth in length and head circumference as estimated from live births at gestational ages from 26 to 42 weeks
9. Cerebral computed tomography in premature infants with an attempt at staging developmental features
10. L‐ carnitine treatment in glutaric aciduria type I
11. Quinolinic acid and other kynurenines in the central nervous system
12. Glutaric aciduria type I misdiagnosed as Leigh's encephalopathy and cerebral palsy