Haemoglobin Q-Thailand and hereditary spherocytosis in a chinese family

Clinical and Laboratory Haematology

Volumn 23, Issue 1, 2001, Pages 53-55

  Leung, K F S ^a   Au, W Y ^a   Chan, A Y Y ^a   Chan, L C ^a   Waye, J S ^b   Chui, D H K ^b   Ma, S K ^a  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b MCMASTER UNIVERSITY   (Canada)

Author keywords

Haemolysis; Hb Q Thailand; Hereditary spherocytosis haemoglobinopathy

Indexed keywords

HEMOGLOBIN ALPHA CHAIN; HEMOGLOBIN Q THAILAND; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 16; FEMALE; GENE DELETION; HEMOGLOBINOPATHY; HEMOLYSIS; HEREDITARY SPHEROCYTOSIS; HETEROZYGOSITY; HUMAN; PRIORITY JOURNAL;

ADULT; ANEMIA, HEMOLYTIC, CONGENITAL; CHINA; FAMILY HEALTH; FEMALE; GENOTYPE; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HUMANS; NUCLEAR FAMILY; OSMOTIC FRAGILITY; PEDIGREE; PHENOTYPE; SPHEROCYTOSIS, HEREDITARY;

EID: 0034949481     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2257.2001.00349.x     Document Type: Article

References (18)

1. The combination of hereditary spherocytosis and heterozygous β thalassaemia: A family study
2. Sphéocytose héréditaire et β thalassémie: Coexistence des deux gènes au sein d'une famille sicilienne
3. A family with sickle cell trait and hereditary spherocytosis
4. Combination of spheroctyosis and a variant of β thalassaemia (isolated raised Hb A2)
5. Hereditary spherocyotosis and thalassaemia
6. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and be-thalassaemia trait: Partial correction of HS phenotype
7. Hereditary spherocytosis: A review of the clinical and molecular aspects of the disease
8. Concurrence of hereditary spherocytosis and alpha thalassaemia
9. The Genetic basis of Hb Q-H disease
10. Interaction of hereditary spherocytosis and alpha thalassaemia: A family study
11. Homozygous sickle cell disease with coexisting hereditary spherocytosis in three siblings
12. Occurrence of hereditary spherocytosis and beta thalassaemia in the same family: Globin chain synthesis and visco diffractometric studies
13. Cellular and membrane properties of α and β thalassemic erythrocytes are different: Implication of differences in clinical manifestations
14. Three inherited intraerythrocytic defects: Hereditary spherocytosis, Hb S and Hb C
15. Alpha-thalassemia and hereditary spherocytosis in the same patient: The interaction of two diseases
16. Recurrent acute splenic sequestration crisis due to interacting genetic defects: Hemoglobin SC disease and hereditary spherocytosis
17. Hereditary spherocytosis and sickle cell trait in the Negro
18. Coexistence of hereditary spherocytosis and β thalassemia: Case report of severe hemolytic anemia in an American black