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[Neonatal polycythaemia and haemoglobin types in infants with G-trisomy (author's transl)].

作者信息

Kohne E, Kleihauer E

出版信息

Klin Wochenschr. 1975 Feb 1;53(3):111-6. doi: 10.1007/BF01466713.

DOI:10.1007/BF01466713
PMID:124798
Abstract

The concentrations of haemoglobin A1, A2, and F were determined quantitatively by column chromatography in 11 newborns with G-trisomy (Down's Syndrome)) and correlated to haematocrit values. In 3 infants the haemoglobin pattern was followed throughout the first six months of life. In connection to the well know polycythaemia, newborns with G-trisomy were found to have significantly higher haemoglobin A1 attaining 35.5 plus or minus 6.6% and A2 equal to 0.79 plus or minus 0.32% as compared to normal infants (HbA1 equal 17.74 plus or minus 4.56%, HbA2 equal to 0.25 plus or minus 0.2%). In G-trisomy the switch-over from synthesis of haemoglobin F to haemoglobin A appears to be initiated earlier than in normal individuals, and it seems even to proceed more rapidly during the first weeks after birth. The amount of adult haemoglobin being synthesized in G-trisomy during the perinatal period may possibly be a response to the increased erythropoiesis, while the influence of chromosomal abnormality seems not to be a specific phenomenon.

摘要

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本文引用的文献

1
Haemoglobin and red cells in the human foetus; III. Foetal and adult haemoglobin.人类胎儿的血红蛋白和红细胞;III. 胎儿血红蛋白与成人血红蛋白
Arch Dis Child. 1955 Apr;30(150):111-6. doi: 10.1136/adc.30.150.111.
2
QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.关于患蒙古症黑人中A2、镰状细胞和胎儿血红蛋白的定量研究,以及对黑人易位型蒙古症的观察
Am J Hum Genet. 1965 Sep;17(5):443-56.
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HUMAN HAEMOGLOBINS.人类血红蛋白
J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.
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FETAL HEMOGLOBIN CONCENTRATION IN THE NEWBORN: INDEX OF MATURITY AND AS SUPPORTIVE EVIDENCE FOR MATERNAL FETAL TRANSFUSION.新生儿的胎儿血红蛋白浓度:成熟度指标及作为母胎输血的支持性证据
Am J Obstet Gynecol. 1965 Jan 1;91:85-8.
5
FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME.13号染色体三体综合征中的胎儿血红蛋白与中性粒细胞异常
Lancet. 1964 Jun 20;1(7347):1363-4. doi: 10.1016/s0140-6736(64)92043-4.
6
HUMAN EMBRYONIC HAEMOGLOBINS.人类胚胎血红蛋白
Nature. 1964 Mar 14;201:1095-7. doi: 10.1038/2011095a0.
7
CONTROLLER-GENE DISEASES: THE OPERON MODEL AS APPLIED TO BETA-THALASSEMIA, FAMILIAL FETAL HEMOGLOBINEMIA AND THE NORMAL SWITCH FROM THE PRODUCTION OF FETAL HEMOGLOBIN TO THAT OF ADULT HEMOGLOBIN.调控基因疾病:应用于β地中海贫血、家族性胎儿血红蛋白病以及从胎儿血红蛋白产生向成人血红蛋白产生正常转换的操纵子模型
J Mol Biol. 1964 Jan;8:128-47. doi: 10.1016/s0022-2836(64)80154-6.
8
[FETAL HEMOGLOBIN IN PRENATAL DYSTROPHY].[产前营养不良中的胎儿血红蛋白]
Helv Paediatr Acta. 1963 Dec;18:554-7.
9
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.染色体三体中的发育性血红蛋白异常:D1三体综合征
Proc Natl Acad Sci U S A. 1964 Jan;51(1):89-97. doi: 10.1073/pnas.51.1.89.
10
Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore.胎儿血红蛋白遗传性持续存在:对巴尔的摩15个黑人家庭中79名患者的研究。
Blood. 1963 Mar;21:261-81.