Natural history of hereditary spherocytosis during the first year of life

Blood

Volumn 95, Issue 2, 2000, Pages 393-397

  Delhommeau, F ^a,b,c   Cynober, T ^a,b,c   Schischmanoff, P O ^a,b,c   Rohrlich, P ^a,b,c   Delaunay, J ^a,b,c   Mohandas, N ^a,b,c   Tchernia, G ^a,b,c  

^a Hôpital Bicêtre   (United States)

^b Bichat hospital Paris   (United States)

^c LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLOOD TRANSFUSION; CONTROLLED STUDY; ERYTHROCYTE MEMBRANE; FAMILY HISTORY; HEMOGLOBIN DETERMINATION; HEMOLYTIC ANEMIA; HEREDITARY SPHEROCYTOSIS; HUMAN; HUMAN CELL; HUMAN EXPERIMENT; HUMAN TISSUE; INFANT MORTALITY; NEWBORN; NORMAL HUMAN; PRACTICE GUIDELINE; PRIORITY JOURNAL; RETICULOCYTE COUNT;

EID: 0034651021     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v95.2.393     Document Type: Article

References (22)

1. Eber SW, Pekrun A, Neufeldt A, Schroter W. Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test. Ann Hematol. 1992; 64:83-92.
2. Godal HC, Heisto H. High prevalence of increased osmotic fragility of red blood cells among Norwegian blood donors. Scand J Hematol. 1981;27:30-34.
3. lolascon A, Perotta S, Tavano R, Miraglia del Giudice E. Hereditary spherocytosis in newboms. In: Bellanti JA, Bracci R, Prindull G, Xanthou M, eds. Neonatal Hematology and Immunology III: Proceedings of the Third Neonatal Hematology and Immunology Symposium, Held in Washington, D.C., September 29-October 1,1996. Amsterdam, Netherlands: Elsevier Science; 1997: 197-202.
4. Lux SE, Palek J. Disorders of the red cell membrane. In Handin RI, Lux SE, Stossel TP, eds. Blood: Principles & Practice of Hematology. New York, NY: Uppincott; 1995:1701-1818.
5. Pinto L, lolascon A, Miraglia del Giudice E, Matarese SMR, Nobili B, Perrotta S. The Italian pédiatrie survey on hereditary spherocytosis. Int J Pediatr Hematol Oncol. 1995:2:43-47.
6. Clark MR, Mohandas N, Shohet SB. Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance. Blood. 1983:61:899-910.
7. Gilsanz F, Ricard MP, Millan I. Diagnosis of hereditary spherocytosis with dual-angle differential light scattering. Am J Clin Pathol. 1993:100:119122.
8. Cynober T, Mohandas N, Tchernia G. Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. J Lab Clin Med. 1996:128:259-269.
9. Michaels LA, Cohen AR, Zhao H, Raphael Rl, Manno CS. Screening for hereditary spherocytosis by use of automated etythrocyte indexes. J Pediatr. 1997;130:957-960.
10. Mohandas N, Kim YR, Tycko DH, Orlik J, Wyatt J, Groner W. Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser scattering. Blood. 1986:68:506-513.
11. Laemmli UK. Cleavage of structural proteins during the assembly of the head of the bacteriophageT4. Nature. 1970:227:680-685.
12. Fairbanks G, Steck TL, Wallach DFH. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 ; 10:2606-2617.
13. Oskl FA. Anemia in the neonatal period. In: Oski FA, Naiman JL Hématologie Problems in the Newborn. 3rd ed. Philadelphia, PA: WB Saunders; 1982:56.
14. Tchemia G, Gauthier F, Mielot F, et al. Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis. Blood. 1993:81:2014-2020.
15. Severin CM. Anatomy of the spleen. In: Pochedly C, Sills RH, Schwarte AD, eds. Disorders of the Spleen: Pathophysiology and Management. New York, NY: Dekker; 1989:1-19.
16. Holroyde CP, Oski FA, Gardner FH. The "pocked" erythrocyte. Red-cell surface alterations in reticuloendothelial immaturity of the neonate. N Engl J Med. 1969:281:516-520.
17. Whitfield CF, Follweiler JB, Lopresti-Morrow L, Miller BA. Deficiency of a-spectrin synthesis in burst-forming units-erythroid in lethal hereditary spherocytosis. Blood. 1991:78:3043-3051.
18. Ribeiro ML, Alloisio N, Almeida H, et al. Hereditary spherocytosis with total absence of band 3 in a baby with mutation Coimbra (V488M) in trie homozygous state [abstract]. Blood. 1997;90:265a.
19. Kling PJ, Schmidt RL, Roberts RA, Widness JA. Serum etythropoietin levels during infancy: associations with erythropoiesis. J Pediatr. 1996:128: 791-796.
20. KaysserTM, Wandersee NJ, Bronson RT, Barker JE. Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis. Blood. 1997:90:4610-4619.
21. Da Costa L, Tchemia G, Sorette M, et al. Mechanistic understanding of spherocyte generation in hereditary spherocytosis and in immune hemolytic anemia. Implications for differential diagnosis based on red cell and reticulocyte indices [abstract]. Blood. 1998;92(suppl 1):9a.
22. Delhommeau F, Cynober T, Mielot F, et al. Hereditary spherocytosis (HS) in newborns and infants: biological diagnosis and preliminary results of Rh-EPO treatment [abstract]. Blood. 1996; 88(suppl1,pt2):139b.