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798 Part VI: The Erythrocyte Chapter 50: Methemoglobinemia and Other Dyshemoglobinemias 799

22. Johnson CJ, Kross BC: Continuing importance of nitrate contamination of groundwa- 59. Hojas-Bernal R, McNab-Martin P, Fairbanks VF, et al: Hb Chile [beta28(B10)Leu—
ter and wells in rural areas. Am J Ind Med 18(4):449, 1990. >Met]: An unstable hemoglobin associated with chronic methemoglobinemia and sul-
23. Chan TY: Food-borne nitrates and nitrites as a cause of methemoglobinemia. Southeast fonamide or methylene blue-induced hemolytic anemia. Hemoglobin 23(2):125, 1999.
Asian J Trop Med Public Health 27(1):189, 1996. 60. Prchal JT, Borgese N, Moore MR, et al: Congenital methemoglobinemia due to methe-
24. Knobeloch L, Proctor M: Eight blue babies. WMJ 100(8):43, 2001. moglobin reductase deficiency in two unrelated American black families. Am J Med
25. Askew GL, Finelli L, Genese CA, et al: Boilerbaisse: An outbreak of methemoglob- 89(4):516, 1990.
inemia in New Jersey in 1992. Pediatrics 94(3):381, 1994. 61. Wild B, Bain BJ: Investigation of abnormal haemoglobins and thalassaemia, in Dacie
26. Bakshi SP, Fahey JL, Pierce LE: Brief recording: Sausage cyanosis—Acquired methemo- and Lewis Practical Haematology, edited by Lewis S, Bain B, Bates I, p 295. Churchill
globinemic nitrite poisoning. N Engl J Med 277(20):1072, 1967. Livingstone, Philadelphia, 2006.
27. Bradberry SM, Whittington RM, Parry DA, et al: Fatal methemoglobinemia due to 62. Yawata Y, Ding L, Tanishima K, et al: New variant of cytochrome b5 reductase defi-
inhalation of isobutyl nitrite. J Toxicol Clin Toxicol 32(2):179, 1994. ciency (b5RKurashiki) in red cells, platelets, lymphocytes, and cultured fibroblasts with
28. Bradberry SM, Gazzard B, Vale JA: Methemoglobinemia caused by the accidental con- congenital methemoglobinemia, mental and neurological retardation, and skeletal
tamination of drinking water with sodium nitrite. J Toxicol Clin Toxicol 32(2):173, 1994. anomalies. Am J Hematol 40(4):299, 1992.
29. Harris JC, Rumack BH, Peterson RG, et al: Methemoglobinemia resulting from absorp- 63. Evelyn K, Malloy H: Microdetermination of oxyhemoglobin, methemoglobin, and
tion of nitrates. JAMA 242(26):2869, 1979. sulfhemoglobin in a single sample of blood. J Biol Chem 126:655, 1938.
30. Lukens JN: Landmark perspective: The legacy of well-water methemoglobinemia. 64. Beutler E: Carboxyhemoglobin, methemoglobin, and sulfhemoglobin determinations,
JAMA 257(20):2793, 1987. in Williams Hematology, edited by Beutler E, Lichtman MA, Coller BS, Kipps TJ, p L50.
31. Stuhlmeier KM, Kao JJ, Wallbrandt P, et al: Antioxidant protein 2 prevents methemo- McGraw-Hill, New York, 1995.
globin formation in erythrocyte hemolysates. Eur J Biochem 270:334, 2003. 65. Halvorsen SM, Dull WL: Phenazopyridine-induced sulfhemoglobinemia: Inadvertent
32. Bewley M, Marohnic C, Barber M: The structure and biochemistry of NADH- rechallenge. Am J Med 91(3):315, 1991.
dependent cytochrome b5 reductase are now consistent. Biochemistry 40:13574, 2001. 66. Watcha MF, Connor MT, Hing AV: Pulse oximetry in methemoglobinemia. Am J Dis
33. Yamada M, Tamada T, Takeda K, et al: Elucidations of the catalytic cycle of NADH- Child 143(7):845, 1989.
cytochrome b5 reductase by X-ray crystallography: New insights into regulation of 67. Molthrop D, Wheeler R, Hall K, et al: Evaluation of the methemoglobinemia associated
efficient electron transfer. J Mol Biol 425(22):4295, 2013. with sulofenur. Invest New Drugs 12:99, 1994.
34. Wang Y, Wu Y, Zheng P, et al: A novel mutation in the NADH-cytochrome b5 reduc- 68. Beutler E, Gelbart T: Carboxyhemoglobin, methemoglobin, and sulf-hemoglobin
tase gene of a Chinese patient with recessive congenital methemoglobinemia. Blood determinations, in Williams Hematology, 4th ed, edited by Williams WJ, Beutler E,
95:3250, 2000. Erslev AJ, Lichtman MA, p 1732. McGraw-Hill, New York, 1990.
35. Shotelersuk V, Tosukhowong P, Chotivitayatarakorn P, et al: A Thai boy with hereditary 69. Barker SJ, Curry J, Redford D, et al: Measurement of carboxyhemoglobin and methe-
enzymopenic methemoglobinemia type II. J Med Assoc Thai 83:1380, 2000. moglobin by pulse oximetry: A human volunteer study. Anesthesiology 105:892, 2006.
36. Jenkins MM, Prchal JT: A novel mutation found in the 3′ domain of NADH- 70. Annabi EH, Barker SJ: Severe methemoglobinemia detected by pulse oximetry. Anesth
cytochrome B5 reductase in an African-American family with type I congenital methe- Analg 108(3):898, 2009.
moglobinemia. Blood 87(7):2993, 1996. 71. Hampson NB: Noninvasive pulse CO-oximetry expedites evaluation and management
37. Nussenzveig RH, Lingam HB, Gaikwad A, et al: A novel mutation of the cytochrome-b5 of patients with carbon monoxide poisoning. Am J Emerg Med 30(9):2021, 2012.
reductase gene in an Indian patient: The molecular basis of type I methemoglobinemia. 72. Beutler E: Red Cell Metabolism: A Manual of Biochemical Methods. Grune & Stratton,
Haematologica 91(11):1542, 2006. New York, 1984.
38. Jenkins M, Prchal J: A high frequency polymorphism of NADH-cytochrome b5 reduc- 73. Board P: NADH-ferricyanide reductase, a convenient approach to the evaluation of
tase in African-Americans. Hum Genet 99:248, 1997. NADH-methaemoglobin reductase in human erythrocytes. Clin Chim Acta 109:233, 1981.
39. Ewenczyk C, Leroux A, Roubergue A, et al: Recessive hereditary methaemoglobi- 74. Lan FH, Tang YC, Huang CH, et al: Antibody-based spot test for NADH-cytochrome
naemia, type II: Delineation of the clinical spectrum. Brain 131(Pt 3):760, 2008. b5 reductase activity for the laboratory diagnosis of congenital methemoglobinemia.
40. Leroux A, Junien C, Kaplan J, et al: Generalised deficiency of cytochrome b5 reductase Clin Chim Acta 273(1):13, 1998.
in congenital methaemoglobinaemia with mental retardation. Nature 258(5536):619, 75. Das Gupta A, Vaidya MS, Bapat JP, et al: Associated red cell enzyme deficiencies and
1975. their significance in a case of congenital enzymopenic methemoglobinemia. Acta Hae-
41. Takeshita M, Tamura M, Kugi M, et al: Decrease of palmitoyl-CoA elongation in plate- matol 64(5):285, 1980.
lets and leukocytes in the patient of hereditary methemoglobinemia associated with 76. Kaftory A, Hegesh E: Improved determination of cytochrome b5 in human erythro-
mental retardation. Biochem Biophys Res Commun 148:384, 1987. cytes. Clin Chem 30(8):1344, 1984.
42. Tanishima K, Tanimoto K, Tomoda A, et al: Hereditary methemoglobinemia due to 77. Gerald PS, George P: Second spectroscopically abnormal methemoglobin associated
cytochrome b5 reductase deficiency in blood cells without associated neurologic and with hereditary cyanosis. Science 129(3346):393, 1959.
mental disorders. Blood 66:1288, 1985. 78. Carrell RW, Kay R: A simple method for the detection of unstable haemoglobins. Br J
43. Maran J, Guan Y, Ou CN, et al: Heterogeneity of the molecular biology of methemoglo- Haematol 23(5):615, 1972.
binemia: A study of eight consecutive patients. Haematologica 90(5):687, 2005. 79. Hutt PJ, Pisciotta AV, Fairbanks VF, et al: DNA sequence analysis proves Hb M-
44. Cohen RJ, Sachs JR, Wicker DJ, et al: Methemoglobinemia provoked by malarial che- Milwaukee-2 is due to beta-globin gene codon 92 (CAC—>TAC), the presumed muta-
moprophylaxis in Vietnam. N Engl J Med 279(21):1127, 1968. tion of Hb M-Hyde Park and Hb M-Akita. Hemoglobin 22(1):1, 1998.
45. Moore MR, Conrad ME, Bradley EL Jr, et al: Studies of nicotinamide adenine dinucle- 80. Darling R, Roughton F: The effect of methemoglobin on the equilibrium between oxy-
otide methemoglobin reductase activity in a Jewish population. Am J Hematol 12(1):13, gen and hemoglobin. Am J Physiol 137:56, 1942.
1982. 81. Johnson CJ, Bonrud PA, Dosch TL, et al: Fatal outcome of methemoglobinemia in an
46. Fine DM, Eyster GE, Anderson LK, et al: Cyanosis and congenital methemoglobinemia infant. JAMA 257(20):2796, 1987.
in a puppy. J Am Anim Hosp Assoc 35(1):33, 1999. 82. Ellis M, Hiss Y, Shenkman L: Fatal methemoglobinemia caused by inadvertent contam-
47. Harvey JW, Ling GV, Kaneko JJ: Methemoglobin reductase deficiency in a dog. J Am Vet ination of a laxative solution with sodium nitrite. Isr J Med Sci 28(5):289, 1992.
Med Assoc 164(10):1030, 1974. 83. Caudill L, Walbridge J, Kuhn G: Methemoglobinemia as a cause of coma. Ann Emerg
48. Lo SC, Agar NS: NADH-methemoglobin reductase activity in the erythrocytes of new- Med 19(6):677, 1990.
born and adult mammals. Experientia 42(11–12):1264, 1986. 84. Clifton J 2nd, Leikin JB: Methylene blue. Am J Ther 10(4):289, 2003.
49. Graubarth J, Bloom CJ, Coleman FC, Solomon, HN. Dye poisoning in the nursery: A 85. Beutler E, Baluda MC: Methemoglobin reduction: Studies of the interaction between
review of seventeen cases. JAMA 128:1155, 1945. cell populations and of the role of methylene blue. Blood 22:323, 1963.
50. Sanchez-Echaniz J, Benito-Fernandez J, Mintegui-Raso S: Methemoglobinemia and 86. Rosen PJ, Johnson C, McGehee WG, et al: Failure of methylene blue treatment in toxic
consumption of vegetables in infants. Pediatrics 107(5):1024, 2001. methemoglobinemia: Associations with glucose-6-phosphate dehydrogenase defi-
51. Hanukoglu A, Danon PN: Endogenous methemoglobinemia associated with diarrheal ciency. Ann Intern Med 75:83, 1971.
disease in infancy. J Pediatr Gastroenterol Nutr 23(1):1, 1996. 87. Bilgin H, Ozcan B, Bilgin T: Methemoglobinemia induced by methylene blue perturba-
52. Hamon I, Gauthier-Moulinier H, Grelet-Dessioux E, et al: Methaemoglobinaemia risk fac- tion during laparoscopy. Acta Anaesthesiol Scand 42(5):594, 1998.
tors with inhaled nitric oxide therapy in newborn infants. Acta Paediatr 99(10):1467, 2010. 88. Kearney TE, Manoguerra AS, Dunford JV Jr: Chemically induced methemoglobinemia
53. Bricker T, Jefferson, LS, Mintz, AA: Methemoglobinemia in infants with enteritis. from aniline poisoning. West J Med 140(2):282, 1984.
J Pediatr 102(1):161, 1983. 89. Harvey J, Keitt A: Studies of the efficacy and potential hazards of methylene blue ther-
54. Murray KF, Christie DL: Dietary protein intolerance in infants with transient methe- apy in aniline-induced methemoglobinemia. Br J Haematol 54:29, 1983.
moglobinemia and diarrhea. J Pediatr 122(1):90, 1993. 90. Coleman MD, Rhodes LE, Scott AK, et al: The use of cimetidine to reduce dapsone-
55. Hegesh E, Hegesh J, Kaftory A: Congenital methemoglobinemia with a deficiency of dependent methaemoglobinaemia in dermatitis herpetiformis patients. Br J Clin Phar-
cytochrome b5. N Engl J Med 314:757, 1986. macol 34:244, 1992.
56. Lehmann H, Huntsman RG: Man’s Haemoglobins. Lippincott, Philadelphia, 1974. 91. Kaplan J, Chirouze M: Therapy of recessive congenital methaemoglobinemia by oral
57. Hayashi A, Fujita T, Fujimura M, et al: A new abnormal fetal hemoglobin, Hb riboflavin. Lancet 2:1043, 1978.
FM-Osaka (alpha 2 gamma 2 63His replaced by Tyr). Hemoglobin 4(3–4):447, 1980. 92. Beutler E: Important recent advances in the field of red cell metabolism: Practical
58. Priest JR, Watterson J, Jones RT, et al: Mutant fetal hemoglobin causing cyanosis in a implications, in Erythrocytes, Thrombocytes, Leukocytes, edited by Gerlach E, Moser K,
newborn. Pediatrics 83(5):734, 1989. Deutsch E, Wilmanns W, p 123. George Thieme Verlag, Stuttgart, 1973.

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