Homozygous β-thalassemia (FCS8-AA) and hereditary spherocytosis in the same patient

Turkish Journal of Haematology

Volumn 18, Issue 2, 2001, Pages 137-141

  Uysal, Z L ^a   Akar, N ^a   Cin, S ^a   Ekici, F ^a   Basak N ^a  

^a ANKARA UNIVERSITY   (Turkey)

Author keywords

Thalassemia; Hereditary spherocytosis

Indexed keywords

CELL MEMBRANE PROTEIN;

ARTICLE; BETA THALASSEMIA; CASE REPORT; CHILD; CODON; DISEASE SEVERITY; ERYTHROCYTE; FAMILIAL INCIDENCE; FAMILY; FAMILY HISTORY; FATHER; FEMALE; FRAMESHIFT MUTATION; HEREDITARY SPHEROCYTOSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MOTHER; OSMOTIC FRAGILITY; SIBLING; TURKEY (REPUBLIC);

EID: 0034966666     PISSN: 13007777     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration osmotic fragility, and autohemolysis
2. Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and β-thalassemia trait; Partial correction HS of phonetype
3. Erythrocyte membrane protein alterations underlying clinical heterogenity in hereditary spherocytosis
4. β thalassemia mutation in the Turkish population
5. The molecular basis of β thalassemia in Turkey
6. The combination of HS and heterozygous. Beta thalassemia: A family study
7. Occurance of hereditary spherocytosis and β thalassemia in the same family: Globin chain synthesis and viscodiffractometric studies
8. Hereditary spherocytosis
9. Hereditary Spherocytosis clinical features, complications and therapy of 22 cases
10. Molecular heterogenity of β-thalassemia intermedia in Turkey