Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 5
77
Views
1
CrossRef citations to date
0
Altmetric
Original Article

A 25-Year Observation of a Japanese Female Patient with Hb Nottingham who has Two Children with the Same Disorder

, , , , , & show all
Pages 446-455 | Received 03 Feb 2012, Accepted 21 Apr 2012, Published online: 19 Sep 2012

REFERENCES

  • Hattori Y. Abnormal hemoglobinopathy. Shounika-Rinsho (in Japanese). 1998;51(10):2077–2086.
  • Gordon-Smith EC, Dacie JV, Blecher TE, French EA, Wiltshire BG, Lehmann H. Hemoglobin Nottingham, βFG 5(98)Val→Gly: a new unstable hemoglobin producing severe hemolysis. Proc R Soc Med. 1973;66(6):507–508.
  • Orringer EP, Felice A, Reese A, . Hb Nottingham (α2β2(FG5)98Val→Gly) in a Caucasian male: clinical and biosynthetic studies. Hemoglobin. 1978;2(4):315–332.
  • Cepreganova B, Wilson JB, Huisman THJ. Hb Nottingham or α2β298(FG5)Val→Gly observed as a de novo mutation in a Canadian child. Hemoglobin 1992;16(1–2):77–79.
  • Brabec V, Indrak K, Fortova H, . Hb Nottingham or α2β298(FG5)Val→Gly in a Czech child. Ann Hematol. 1994;69(2):93–95.
  • Memtsoudis SG, Lekowski RW Jr, Rosenberger P, . Pulmonary thrombectomy in a patient with Hemoglobin Nottingham. Perfusion. 2007;22(4):299–301.
  • Ohba Y. Unstable hemoglobins. Hemoglobin. 1990;14(4):353–388.
  • Hattori Y. The techniques of hemoglobin analysis. In: Asano S, Ed. Miwa Hematology, 3rd ed. Tokyo: Bunko-Do (in Japanese). 2006:1922–1933.
  • Basset P, Beuzard Y, Garel MC, Rosa J. Isoelectric focusing of human hemoglobin: its application to screening, to the characterization of 70 variants, and to the study of modified fractions of normal hemoglobins. Blood. 1978;51(5):971–982.
  • Hattori Y. A new unstable Hemoglobin Iwata, F8 (α87) His→Arg. Bull Yamaguchi Med Sch. 1980;27(3–4):65–83.
  • Ohba Y. Hb Köln in Japan. Yamaguchi Med J (in Japanese). 1983;32(1):105–117.
  • Ando C, Moriyama K, Nakashima Y, . Unstable hemoglobinemia, Hb Buenos Aires, Bryn Mawr, followed up for eighteen years. Fukuoka Acta Med. 2004;95(11):297–304.
  • Wajcman H, Galactéros F. Abnormal hemoglobins with high oxygen affinity and erythrocytosis. Hematol Cell Ther. 1996;38(4):305–312.
  • Wajcman H, Galactéros F. Hemoglobins with high oxygen affinity leading to erythrocytosis. New variants and new concepts. Hemoglobin. 2005;29(2):91–106.
  • González Fernández FA, Villegas A, Ropero P, . Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group. Ann Hematol. 2009;88(3):235–238.
  • Durakbasa CU, Timur C, Sehiralti V, Mutus M, Tosyali N, Yoruk A. Pediatric splenectomy for hematological diseases: outcome analysis. Pediatr Surg Int. 2006;22(8):635–639.
  • Khan PN, Nair RJ, Olivares J, Tingle LE, Li Z. Postsplenectomy reactive thrombocytosis. Proc (Bayl Univ Med Cent). 2009;22(1):9–12.
  • Ataga KI, Cappellini MD, Rachmilewitz EA. β-Thalassaemia and sickle cell anaemia as paradigms of hypercoagulability. Br J Haematol. 2007;139(1):3–13.
  • Boas FE, Forman L, Beutler E. Phosphatidylserine exposure and red cell viability in red cell aging and in hemolytic anemia. Proc Natl Acad Sci USA. 1998;95(6):3077–3081.
  • Kanno H. Critical role of phosphatidylserine in hemolysis due to red blood cell enzyme/membrane defects. Nippon Rinsho (in Japanese). 2008;66(3):461–468.
  • Shulman LP, Phillips OP, Tolley E, Sammons D, Wachtel SS. Frequency of nucleated red blood cells in maternal blood during the different gestational ages. Hum Genet. 1998;103(6):723–726.
  • Singounas EG, Sakas DE, Hadley DM, . Paraplegia in a pregnant thalassemic woman due to extramedullary hematopoiesis: successful management with transfusions. Surg Neurol. 1991;36(3):210–215.
  • Konstantopoulos K, Plataniotis G, Maris T, . Extramedullary haemopoiesis in thalassaemia intermedia: an unusual case of relapsing paraparesis in pregnancy. Haematologia (Budap). 1995;27(1):29–32.
  • Phupong V, Uerpairojkij B, Limpongsanurak S. Spinal cord compression: a rareness in pregnant thalassemic women. J Obstet Gynaecol Res. 2000;26(2):117–120.
  • Savona-Venture C, Bonello F. β-Thalassemia syndromes and pregnancy. Obstet Gynecol Surv. 1994;49(2):129–137.
  • Nassar AH, Usta IM, Rechdan JB, Koussa S, Inati A, Taher AT. Pregnancy in patients with β-thalassemia intermedia: outcome of mothers and newborns. Am J Hematol. 2006;81(7):499–502.
  • Boldrini R, Bozzola C, Gallarotti E, Ribaldone R. Fatal splenic rupture in a pregnant woman with Hemoglobin C/β-thalassemia and myeloid metaplasia. Arch Pathol Lab Med. 2006;130(8):1231–1232.
  • Al Jama FE, Gasem T, Burshaid S, Rahman J, Al Suleiman SA, Rahman MS. Pregnancy outcome in patients with homozygous sickle cell disease in a university hospital, Eastern Saudi Arabia. Arch Gynecol Obstet. 2009;280(5):793–797.
  • Cheung VY, Silverman JA. Hemoglobin Köln and pregnancy. J Obstet Gynaecol Can. 2008;30(10):907–909.
  • Bauer C, Jelkmann W, Moll W. High oxygen affinity of maternal blood reduces fetal weight in rats. Respir Physiol. 1981;43(2):169–178.
  • Bard H, Rosenberg A, Huisman THJ. Hemoglobinopathies affecting maternal-fetal oxygen gradient during pregnancy: molecular, biochemical and clinical studies. Am J Perinatol. 1998;15(6):389–393.
  • Yamada K. Abnormal hemoglobinopathies. Shounika-MOOK (in Japanese). 1982;25:169–180.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.