Erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS)

British Journal of Haematology

Volumn 110, Issue 4, 2000, Pages 998-1001

  Zdebska, E ^a   Wozniewicz, B ^a   Adamowicz Salach, A ^a   Koscielak, J ^a  

^a INSTITUTE OF HEMATOLOGY AND TRANSFUSION MEDICINE   (Poland)

Author keywords

Band 3; Congenital dyserythropoietic anaemia type I; Glycosphingolipids; Hypoglycosylation; Polyglycosylceramides

Indexed keywords

ERYTHROCYTE BAND 3 PROTEIN; GLYCOCONJUGATE; GLYCOSPHINGOLIPID; CERAMIDE POLYGLYCOSIDE; LACTOTRIAOSYLCERAMIDE; NEOLACTOTRIAOSYLCERAMIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBOHYDRATE ANALYSIS; CASE REPORT; CLASSIFICATION; COMPARATIVE STUDY; CONGENITAL DYSERYTHROPOIETIC ANEMIA; ERYTHROCYTE MEMBRANE; FEMALE; HUMAN; METABOLISM; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DISEASE COURSE; DYSERYTHROPOIESIS; ERYTHROBLAST; ERYTHROCYTE STRUCTURE; GLYCOSYLATION; HEREDITARY HEMOLYTIC ANEMIA; HUMAN TISSUE; PRIORITY JOURNAL;

ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; CARBOHYDRATE SEQUENCE; ERYTHROCYTE MEMBRANE; FEMALE; GLYCOCONJUGATES; GLYCOSPHINGOLIPIDS; HUMANS;

EID: 0033623427     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2000.02288.x     Document Type: Article

References (12)

1. Carbohydrate-deficient glycoprotein syndrome type II - An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity with a positive acidified-serum lysis test (HEMPAS)
2. Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: A type of congenital dyserythropoietic anaemia
3. HEMPAS
4. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q 11.2 by genomewide search
5. Congenital dyserythropoietic anaemia with karyorrhexis and multinuclearity of erythroblasts
6. Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)
7. New method for the isolation of polyglycosylceramides from human erythrocyte membranes
8. Localization of the gene for congenital dyserythropoietic anemia type I to chromosome15q15.1-15.3
9. Congenital dyserythropoietic anaemias: Clinical features, haematological morphology an new biochemical data
10. A single-sample method for determination of carbohydrate and protein contents of glycoprotein bands separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis
11. Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II)
12. Band 3 glycoprotein and glycophorin A from erythrocytes of children with CDG-Ia are underglycosylated