Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 10356134.
- Also identified by PMC identifier 7095022.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Leukocyte adhesion deficiency II has been described in only 2 patients; herein we report extensive investigation of another patient. The physical stigmata were detected during prenatal ultrasonographic investigation. Sialyl-Lewis X (sLex) was absent from the surface of polymorphonuclear neutrophils, and cell binding to E- and P-selectin was severely impaired, causing an immunodeficiency. The elevation of peripheral neutrophil counts occurred within several days after birth. A severe hypofucosylation of glycoconjugates bearing fucose in different glycosidic links was present in all cell types investigated, demonstrating that leukocyte adhesion deficiency II is not only a disorder of leukocytes but a generalized inherited metabolic disease affecting the metabolism of fucose.
Medical subject headings
- Carbohydrate Metabolism, Inborn Errors
- Fucose
- Leukocyte-Adhesion Deficiency Syndrome