Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India
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Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K (2008) Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test 12(2):177–180
Embury SH, Dozy AM, Miller J, Davis JR, Kleman KM, Preisler H, Vichinsky E, Lande WN, Lubin BH, Kan YW, Mentzer WC (1982) Concurrent sickle-cell anemia and alpha thalassemia: effect on severity of anemia. N Engl J Med 306(5):270–274
Steinberg MH, Rosenstock W, Coleman MB, Adams JG, Platica O, Cedeno M, Rieder RF, Wilson JT, Milner P, West S (1984) Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood 63(6):1353–1360
Bain BJ, Lewis SM, Bates I (2006) Basic hematological techniques. In: Lewis SM, Bain BJ, Bates I (eds) Dacie and Lewis practical hematology, 10th edn. Churchill Livingstone, Philadelphia, p 25
Colah RB, Gorakshakar AC, Lu CY, Nadkarni AH, Desai SN, Pawar AR, Lulla CP, Krishnamoorthy R, Mohanty D (1997) Application of covalent reverse dot blot hybridisation for rapid prenatal diagnosis of the common Indian thalassemia syndromes. Ind J Hematol Blood Transf 15(1):10–13
Tan AS, Quah TC, Low PS, Chong SS (2001) A rapid and reliable 7 deletion multiplex polymerase chain reaction assay for α thalassemia. Blood 98(1):250–251
Tritipsombut J, Sanchaisuriya K, Fucharoen S, Fucharoen G, Siriratmanawong N, Pinmuang-ngam C, Sanchaisuriya P (2008) Hemoglobin profiles and hematologic features of thalassemic newborns: application to screening of alpha-thalassemia 1 and hemoglobin E. Arch Pathol Lab Med 132(11):1739–1745
Charoenkwan P, Taweephol R, Sirichotiyakul SI, Tantiprabha Sae-Tung WR, Suanta S (2010) Cord blood screening for α- thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters. Blood Cell Mol Dis 45(1):53–57
Quadri MI, Islam SI, Nasserullah Z (2000) The effect of α-thalassemia on cord blood red cell indices and interaction with sickle cell gene. Ann Saudi Med 20(5–6):367–370
Al Kindi S, Al Zadjali S, Al Madhani A, Daar S, Al Haddabi H, Al Abri Q, Gravell D, Berbar T, Pravin S, Pathare A, Krishnamoorthy R (2010) Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates. Hemoglobin 34(2):135–144
Wong P, Weerakul P, Sritippayawan S (2016) Hemoglobin analysis in the first year of life. Mediterr J Hematol Infect Dis 8(1):e2016012
Tanphaichitr VS, Pung-amritt P, Puchaiwatananon O, Winichagoon P, Fucharoen S, Suvatte V, Wasi P (1987) Studies of hemoglobin Bart’s and deletion of alpha-globin genes from cord blood in Thailand. Birth Defects Orig Artic Ser 23(5A):15–21
Kyriacou K, Kyrri A, Kalogirou E, Vasiliades P, Angastiniotis M, Ioannou PA, Kleanthous M (2000) Hb Bart’s levels in cord blood and alpha-thalassemia mutations in cyprus. Hemoglobin 24(3):171–180
Rugless MJ, Fisher CA, Stephens AD, Amos RJ, Mohammed T, Old JM (2006) Hb Bart’s in cord blood: an accurate indicator of alpha-thalassemia. Hemoglobin 30(1):57–62
Uaprasert N, Settapiboon R, Amornsiriwat S, Sarnthammakul P, Thanapat T, Rojnuckarin P, Sutcharitchan P (2014) Diagnostic utility of isoelectric focusing and high performance liquid chromatography in neonatal cord blood screening for thalassemia and non-sickling haemoglobinopathies. Clin Chim Acta 427(1):23–26