Demonstration and quantification of "hyperchromic" erythrocytes by haematological analysers. Application to screening for heredity and acquired spherocytosis

Clinical Laboratory

Volumn 48, Issue 3-4, 2002, Pages 163-170

  Kutter, Dolphe ^a   Coulon, Nathalie ^a   Stirn, Fernand ^a   Thoma, Martine ^a   Janecki, Jerzy ^a  

^a Laboratoires Reunis Kutter Lieners Hastert Centre Langwies   (Luxembourg)

Author keywords

ADVIA 120 haematological analyser; Cryohaemolysis test; Erythrocyte hyperchromia; Spherocytosis

Indexed keywords

HEMOGLOBIN;

ANALYZER; ARTICLE; ARTIFACT; AUTOMATION; BLOOD ANALYSIS; CELL VOLUME; CONTROLLED STUDY; COST; DIFFRACTION; HEMOGLOBIN DETERMINATION; HEMOLYSIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HUMAN CELL; LASER; MAJOR CLINICAL STUDY; SCREENING; SPHEROCYTOSIS;

ANEMIA, HEMOLYTIC; ERYTHROCYTE COUNT; ERYTHROCYTES, ABNORMAL; FEMALE; HEMATOLOGIC TESTS; HUMANS; MALE; PREGNANCY; SPECTRUM ANALYSIS; SPHEROCYTES; SPHEROCYTOSIS, HEREDITARY;

EID: 0036207656     PISSN: 14336510     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (22)

1. Abnormal and double erythrocyte populations revealed by the "erythrogram" of haematological analysers
2. Les maladies héréditaires de la membrane érythrocytaire: Du tableau clinique aux mécanismes génétiques eet moléculaires sous-jacents
3. Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity
4. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
5. Ankyrin deficiency is the most common defect in dominant and non-dominant hereditary spherocytosis
6. Visual analysis of the distribution of large sets of laboratory results (in Polish)
7. Usefulness of the Cryohemolysis test in the diagnosis of hereditary spherocytosis
8. Hemolytic anemia in patients receiving sulfalazine
9. Hemolysis during salicylazosulfapyridine therapy
10. Autoimmune haemolytic anaemia associated with ulcerative colitis
11. Auto-immune haemolytic anaemia in ulcerative colitis
12. Hereditary spherocytosis is more common than expected. Hemolysis, anemia and splenomegaly are among the symptoms
13. High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors
14. Prevalence of increased osmotic fragility of erythrocytes in German blood donors - Screening using a modified glycerol lysis test
15. Silent forms of hereditary spherocytosis
16. Clinical and molecular evaluation of non-dominant hereditary spherocytosis
17. The diagnosis and management of hereditary spherocytosis
18. Hematologically important mutations: Spectrin and ankyrin variant in hereditary spherocytosis
19. Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency
20. Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil
21. Hereditary spherocytosis, ellliptocytosis and related disorders