Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

American Journal of Ophthalmology

Volumn 123, Issue 6, 1997, Pages 846-848

  Lawlor, D P ^a   Kalina, R E ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL ENZYME; OXIDOREDUCTASE;

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FEMALE; HUMAN; OPHTHALMOSCOPY; PIGMENT EPITHELIUM; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA PIGMENT DEGENERATION;

EID: 0030986606     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(14)71141-9     Document Type: Article

References (4)

1. Pollitt RJ Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death Padiatr Padol 28 1993 13 17
2. Bertini E Dionisi-Vici C Garavaglia B Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency Eur J Pediatr 151 1992 121 126
3. Sewall AC Bender SW Wirth S Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder Eur J Pediatr 153 1994 745 750
4. Glasgow BJ Brown HH Hannah JB Foos RY Ocular pathologic findings in neonatal adrenoleukodystrophy Ophthalmology 94 1987 1054 1060