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Predictive value of cord blood hematological indices and hemoglobin Barts for the detection of heterozygous alpha-thalassemia-2 in an African-Caribbean population.
van der Dijs FP, Volmer M, van Gijssel-Wiersma DG, Smit JW, van Veen R, Muskiet FA. van der Dijs FP, et al. Clin Chem. 1999 Sep;45(9):1495-500. Clin Chem. 1999. PMID: 10471652
BACKGROUND: Cord blood hemoglobin Barts (HbBarts) and hemocytometric indices may be used for classification of newborns into those without alpha-thalassemia-2 (alphaalpha/alphaalpha) and with heterozygous alpha-thalassemia-2 (-alpha(3.7)/alphaalpha). ...
BACKGROUND: Cord blood hemoglobin Barts (HbBarts) and hemocytometric indices may be used for classification of newborns into t …
Spurious hemoglobin Barts caused by bilirubin: a common interference mimicking an uncommon hemoglobinopathy.
Howanitz PJ, Kozarski TB, Howanitz JH, Chauhan YS. Howanitz PJ, et al. Am J Clin Pathol. 2006 Apr;125(4):608-14. doi: 10.1309/73WJ-V2E0-RTVQ-H0BB. Am J Clin Pathol. 2006. PMID: 16627270
Our objective was to identify unknown tall peaks with elution times and shapes of hemoglobin Barts found on hemoglobin chromatograms that could not be confirmed by alkaline and acid gel electrophoresis. ...Regression of the height of the unknown peaks to serum bilir …
Our objective was to identify unknown tall peaks with elution times and shapes of hemoglobin Barts found on hemoglobin chromat …
A fast hemoglobin variant on newborn screening is associated with alpha-thalassemia trait.
Miller ST, Desai N, Pass KA, Rao SP. Miller ST, et al. Clin Pediatr (Phila). 1997 Feb;36(2):75-8. doi: 10.1177/000992289703600203. Clin Pediatr (Phila). 1997. PMID: 9118593
Alpha thalassemia trait (alpha-thal-1) is a common cause of microcytosis in black and Asian populations. A small amount of hemoglobin Barts (2-8%) is transiently present in affected infants at birth and detectable in many newborn screening laboratories; it is a fast …
Alpha thalassemia trait (alpha-thal-1) is a common cause of microcytosis in black and Asian populations. A small amount of hemoglobin …
Rapid identification of the copy number of α-globin genes by capillary electrophoresis analysis.
Liao YM, Lin SK, Liu TC, Chiou SS, Lu HC, Kao CF, Chang JG. Liao YM, et al. Clin Biochem. 2012 Jul;45(10-11):798-805. doi: 10.1016/j.clinbiochem.2012.02.006. Epub 2012 Feb 21. Clin Biochem. 2012. PMID: 22374170
Moreover, a low amount of maternal cell contamination in the fetus specimen for the prenatal diagnosis of hemoglobin Barts hydrops fetalis as well as the rare multiplicated alpha-globin genes can be identified using this method. ...
Moreover, a low amount of maternal cell contamination in the fetus specimen for the prenatal diagnosis of hemoglobin Barts hyd …
Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).
Al-Allawi NA, Shamdeen MY, Rasheed NS. Al-Allawi NA, et al. Ann Saudi Med. 2010 Mar-Apr;30(2):153-5. doi: 10.4103/0256-4947.60523. Ann Saudi Med. 2010. PMID: 20220267 Free PMC article.
Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of alpha-thalassemia. ...At 32 weeks, intrauterine death was detected. Molecular studies revealed that the fetus had the hemoglobin Barts hydrops fetali …
Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of alpha-thalassemia. ...A …
Effect of fetal diagnosis on the outcomes of second-trimester pregnancy termination for fetal abnormalities: a pilot study.
Lo TK, Lau WL, Lai FK, Lam HS, Tse HY, Leung WC, Chin RK. Lo TK, et al. J Matern Fetal Neonatal Med. 2008 Aug;21(8):523-7. doi: 10.1080/14767050802104835. J Matern Fetal Neonatal Med. 2008. PMID: 18609362
METHODS: This was a retrospective review of cases undergoing second-trimester pregnancy termination for the fetal diagnoses of hemoglobin Barts, trisomy 21, and trisomy 18 during the period from 1999 to 2006. ...After adjusting for maternal age, parity, history of c …
METHODS: This was a retrospective review of cases undergoing second-trimester pregnancy termination for the fetal diagnoses of hemoglobin …
Hemoglobin barts hydrops fetalis syndrome.
Bowman E, Watts J, Burrows R, Chui DH. Bowman E, et al. Haematologia (Budap). 1987;20(3):125-30. Haematologia (Budap). 1987. PMID: 3692334