Isolated sulfite oxidase deficiency: MR imaging features

American Journal of Neuroradiology

Volumn 23, Issue 3, 2002, Pages 484-485

  Dublin, Arthur B ^a   Hald, John K ^a   Wootton Gorges, Sandra L ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SULFITE OXIDASE; SULFUR AMINO ACID;

ARTICLE; AUTOSOMAL DISORDER; BRAIN METABOLISM; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DIAGNOSTIC PROCEDURE; DISEASE COURSE; ENZYME DEFICIENCY; FEMALE; HUMAN; METABOLIC DISORDER; NEUROLOGIC DISEASE; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; TIME SERIES ANALYSIS;

AMINO ACID METABOLISM, INBORN ERRORS; BRAIN; DISEASE PROGRESSION; FEMALE; HUMANS; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; OXIDOREDUCTASES ACTING ON SULFUR GROUP DONORS; SEIZURES;

EID: 0036130408     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Molybdenum cofactor deficiency, isolated sulfite oxidase deficiency
2. Isolated sulfite oxidase deficiency
3. Isolated sulfite oxidase deficiency: Review of two cases in one family
4. A mild form of infantile isolated sulphite oxidase deficiency
5. Sulfite oxidase deficiency: Clinical, neuroradiologic, and biochemical features in two new patients
6. Sulfite oxidase deficiency presenting as Leigh syndrome
7. Molybdenum cofactor deficiency-phenotypic variability in a family with a late-onset variant
8. Infantile isolated sulphite oxidase deficiency: Report of a case with negative sulphite test and normal sulphate excretion
9. Cytochrome oxidase deficiency presenting as birth asphyxia