Anaemia and thrombocytopenia due to haemophagocytosis in a 7-month-old boy with galactosialidosis

Journal of Inherited Metabolic Disease

Volumn 21, Issue 6, 1998, Pages 679-680

  Olcay, L ^a   Gumruk F ^a   Boduroglu K ^a   Coskun T ^a   Tuncbilek E ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ANEMIA; ARTICLE; CASE REPORT; GALACTOSIALIDOSIS; HEMOPHAGOCYTIC SYNDROME; HUMAN; INFANT; MALE; THROMBOCYTOPENIA;

ANEMIA; BETA-GALACTOSIDASE; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; INFANT; MALE; METABOLISM, INBORN ERRORS; NEURAMINIDASE; PHAGOCYTOSIS; THROMBOCYTOPENIA;

EID: 0031783123     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005444903597     Document Type: Article

References (2)

1. d'Azzo A, Andria G, Strisciuglio P, Galjaard H (1995) Galactosialidosis. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill, 2825-2837.
2. Yüce A, Koçak N, Besley GT (1996) Galactosialidosis in two siblings. Turk J Pediatr 38: 85-89.