根据血型在卡塔尔省血红蛋白病

Qassim Jawell Odah, Rawaa Kamel Abd, Sameeha Naser Abd
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引用次数: 2

摘要

血红蛋白病是一组通过血红蛋白分子产生或结构异常的家庭获得的疾病,引起相当大的公共卫生问题。全球乙肝病毒携带者估计为2.69亿人,每年约有40万新生儿。因此,受影响儿童的出生不仅给受影响儿童及其家庭,而且给整个社会和国家带来了广泛的身体、生理和财政负担。方法:在这项横断面研究中,601例血红蛋白病患者(男性317例,女性284例),年龄从几个月到≥40岁。在数据收集期间(2016年3月1日至5月31日),他们在Thi-Qar省Al- Habobi医院的遗传性血液病中心就诊。结果:地中海贫血的患病率高于其他血清病(76.53),以o型血居多,以≤10岁人群高发(54.08),其次为21 ~ 30岁人群(34.44),城市高发(60.90)。建议:应采取充分和适当的治疗和预防措施,以减少受影响儿童的出生,如对个人进行健康教育,使其了解对所有夫妇进行婚前筛查以确定血红蛋白病基因携带者个体的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemoglobinopathies According To Blood Groups In Thi-Qar Governorate
The hemoglobinopathies are a group of disorders that acquired through families in which there is abnormal creation or structure of the hemoglobin molecule, which cause a considerable public health problem. The carriers of Hb diseases worldwide are estimated to be 269 million with about 400,000 births a year.  The birth of effected child, consequently, places extensive physical, physiological and fiscal burden, not only on the affected child and its family, but also on the society and the nation at large. Methodology: In this cross- sectional study 601 patients with hemoglobinopathies  (317 males and 284 females), Whose  age ranged from months to ≥40 years. They were attending genetic blood disease center at Al- Habobi hospital in Thi-Qar governorate during the data collection period (1st March to 31 May 2016). Results: Thalassemia has high prevalence than other hemoblobinopathies (76.53) and majority of cases was blood group O. The highly percentage of cases was at age ≤ 10 years (54.08) followed by 21-30 years was (34.44), highly percentage of cases was in urban (60.90). Recommendations: Adequate and suitable therapeutic and preventive measures should be taken to diminish birth of effected children such as health education of individuals about importance of premarital screening program for all couple to identify gen carrier individual of hemoglobinopathies.
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