Neonatal anemia associated with Southeast Asian Ovalocytosis

International Journal of Hematology

Volumn 82, Issue 3, 2005, Pages 201-205

  Laosombat, Vichai ^a   Dissaneevate, Supaporn ^a   Wongchanchailert, Malai ^a   Satayasevana, Benjamas ^a  

^a PRINCE OF SONGKLA UNIVERSITY   (Thailand)

Author keywords

Anemia; Hyperbilirubinemia; Newborn; SAO; Southeast Asian ovalocytosis

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE; HEMOGLOBIN; HEMOGLOBIN E;

ALPHA THALASSEMIA; ARTICLE; AUTOANALYZER; BLOOD GROUP ABO INCOMPATIBILITY; BLOOD SMEAR; BLOOD TRANSFUSION; CELL TYPE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA DETERMINATION; ELLIPTOCYTOSIS; ERYTHROCYTE; ERYTHROCYTE COUNT; ERYTHROCYTE VOLUME; FEMALE; FETOMATERNAL TRANSFUSION; GENE DELETION; GLYCOGEN STORAGE DISEASE TYPE 1; HEMATOCRIT; HEMATOLOGY; HEMOGLOBIN DETERMINATION; HEMOLYSIS; HUMAN; HUMAN CELL; HYPERBILIRUBINEMIA; JAUNDICE; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MEAN CORPUSCULAR HEMOGLOBIN; NEWBORN; NEWBORN ANEMIA; OVALOCYTE; PALLOR; PHOTOTHERAPY; POLYMERASE CHAIN REACTION; PREMATURITY; RETICULOCYTE; SOUTHEAST ASIAN OVALOCYTOSIS; STOMATOCYTE; SYPHILIS; THETA CELL;

ANEMIA, NEONATAL; ASIA, SOUTHEASTERN; ELLIPTOCYTOSIS, HEREDITARY; FEMALE; GENE DELETION; HUMANS; INFANT, NEWBORN; JAUNDICE, NEONATAL; MALE; RETICULOCYTE COUNT; RETROSPECTIVE STUDIES;

EID: 27644515941     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1532/IJH97.A20505     Document Type: Article

References (22)

1. Blanchette VS, Zipursky A. Assessment of anemia in newborn infants. Clin Perinatol. 1984;11:489-510.
2. Gill FM, Schwartz E. Anemia in early infancy. Pediatr Clin North Am. 1972;19:841-853.
3. Laosombat V, Dissaneevate S, Peerapittayamongkol C, Matsuo M. Neonatal hyperbilirubinemia associated with Southeast Asian ovalocytosis. Am J Hematol. 1999;60:136-139.
4. Austin RF, Desforges JF. Hereditary elliptocytosis: an unusual presentation of hemolysis in the newborn associated with transient morphologic abnormalities. Pediatrics. 1969;44:196-200.
5. Harrison KL, Collins KA, McKenna HW. Hereditary elliptical stomatocytosis: a case report. Pathology. 1976;8:307-311.
6. Honig GR, Lacson PS, Maurer HS. A new familial disorder with abnormal erythrocyte morphology and increased permeability of the erythrocytes to sodium and potassium. Pediatric Res. 1971;5: 159-166.
7. Palek J. Introduction: red blood cell membrane proteins, their genes and mutations. Semin Hematol. 1993;30:1-3.
8. Mgone CS, Koki G, Paniu MM, et al. Occurrence of the erythrocyte band 3 (AE1) gene deletion in relation to malaria endemicity in Papua New Guinea. Trans R Soc Trop Med Hyg. 1996;90:228-231.
9. Jarolim P, Palek J, Amato D, et al. Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis. Proc Natl Acad Sci U S A. 1991;88:11022-11026.
10. Jay DG. Role of band 3 in homeostasis and cell shape. Cell. 1996; 86:853-854.
11. Amato D, Booth PB. Hereditary ovalocytosis in Melanesians. P N G Med J. 1977;20:26-32.
12. Reardon DM, Seymour CA, Cox TM, Pinder JC, Schofield AE, Tanner MJ. Hereditary ovalocytosis with compensated haemolysis. Br J Haematol. 1993;85:197-199.
13. O'Donnell A, Allen SJ, Mgone CS, Martinson JJ, Clegg JB, Weatherall DJ. Red cell morphology and malaria anaemia in children with Southeast-Asian ovalocytosis band 3 in Papua New Guinea. Br J Haematol. 1998;101:407-412.
14. Noparatana C, Noparatana C, Kanjanaopas S, Saechan V, Matsuo M. Southeast Asian ovalocytosis (SAO) in the south of Thailand. Paper presented at: PSU-ICMR Symposium; July 25-26, 1996; Songkla, Thailand (abstract 18).
15. Tanphaichitr VS, Pung-amritt P, Puchaiwatananon O, et al. Studies of hemoglobin Bart's and deletion of alpha-globin genes from cord blood in Thailand. Birth Defects Orig Artic Ser. 1987;23:15-21.
16. Pootrakul S, Wasi P, Na-Nakorn S. Studies on haemoglobin Bart's in Thailand: the incidence and the mechanism of occurrence in cord blood. Ann Hum Genet. 1967;31:149.
17. Sae-Ung N, Fucharoen G, Fucharoen S. Expression of hemoglobin E in newborn. Southeast Asian J Trop Med Public Health. 1995; 26(suppl 1):246-248.
18. Pung-Amritt P, Tanphaichitr VS, Tachavanich K, Suwantol L, Glomglao W. Prevalence of HbE from cord blood samples and after one year follow-up. Southeast Asian J Trop Med Public Health. 1999;30(suppl 2):97-99.
19. Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group. Bull World Health Organ. 1989;67:601-611.
20. Practice parameter: management of hyperbilirubinemia in the healthy term newborn. American Academy of Pediatrics. Provisional Committee for Quality Improvement and Subcommittee on Hyperbilirubinemia. Pediatrics. 1994;94:558-565.
21. Kling PJ, Schmidt RL, Roberts RA, Widness JA. Serum erythropoietin levels during infancy: associations with erythropoiesis. J Pediatr. 1996;128:791-796.
22. Sutomo R, Laosombat V, Sadewa AH, et al. Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome. Pediatr Int. 2002;44:427-432.