An unusual case of multiple carboxylase deficiency presenting as generalized pustular psoriasis in a Chinese boy

Journal of Inherited Metabolic Disease

Volumn 20, Issue 1, 1997, Pages 106-107

  Law, L K ^a,e   Lau, C Y ^a,b   Pang, C P ^a   Lam, W Y ^c   Sweetman, L ^d   Fok, T F ^a   Hjelm, M ^a  

^a CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^b YAN CHAI HOSPITAL   (Hong Kong)

^c TUEN MUN HOSPITAL   (Hong Kong)

^d CHILDREN S HOSPITAL LOS ANGELES   (United States)

^e CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLASE;

CASE REPORT; CHILD; CHINESE; ENZYME DEFICIENCY; HUMAN; MALE; PRESCHOOL CHILD; PUSTULAR PSORIASIS; REVIEW;

ASIAN CONTINENTAL ANCESTRY GROUP; HUMANS; INFANT; MALE; MULTIPLE CARBOXYLASE DEFICIENCY; PSORIASIS;

EID: 0031042422     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005382112066     Document Type: Review

References (3)

1. Barker JNWN (1991) The pathophysiology of psoriasis. Lancet 338: 227 - 234
2. Dove Pettit DA, Wolf B (1991) Quantitative colorimetric assay of biotinidase activity. In Hommes FA, ed. Techniques in Diagnostic Human Biochemical Genetics. A Laboratory Manual. New York: Wiley-Liss, 561 - 566.
3. Wolf B (1995) Disorders of biotin metabolism. In Seriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 3151 - 3177.