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血红蛋白E:东南亚裔儿童中常见的血红蛋白病。

Hemoglobin E: a common hemoglobinopathy among children of Southeast Asian origin.

作者信息

Katsanis E, Luke K H, Hsu E, Yates J R

出版信息

CMAJ. 1987 Jul 1;137(1):39-42.

Abstract

With the recent immigration of Southeast Asians to Canada, hemoglobin E has become a frequent diagnosis. The clinical and hematologic findings in 42 children (mean age 4.3 years) with hemoglobin E are presented. There were 33 heterozygotes (having hemoglobin E trait), 6 homozygotes (having hemoglobin EE) and 3 double heterozygotes (having hemoglobin E-beta-thalassemia). The heterozygotes had low-normal hemoglobin levels and mean corpuscular volumes; coexisting iron deficiency, present in 62% of these children, resulted in substantially lower hemoglobin levels, very low mean corpuscular volumes and lower than expected levels of hemoglobin E on electrophoresis. The children with hemoglobin EE were only slightly anemic, but those with hemoglobin E-beta-thalassemia had severe anemia and required long-term transfusion therapy. Nutritional factors and parasitic infestations were the main causes of iron depletion, which was common, particularly in children less than 2 years old (87%). Physicians of patients of Southeast Asian origin should be aware of the clinical and hematologic presentation of these hemoglobinopathies.

摘要

随着近期东南亚人移民到加拿大,血红蛋白E已成为一种常见的诊断疾病。本文介绍了42名血红蛋白E患儿(平均年龄4.3岁)的临床和血液学表现。其中有33名杂合子(具有血红蛋白E性状)、6名纯合子(具有血红蛋白EE)和3名双重杂合子(具有血红蛋白E-β地中海贫血)。杂合子的血红蛋白水平和平均红细胞体积略低于正常;62%的患儿同时存在缺铁情况,这导致血红蛋白水平大幅降低、平均红细胞体积极低以及电泳时血红蛋白E水平低于预期。血红蛋白EE患儿仅有轻度贫血,但血红蛋白E-β地中海贫血患儿有严重贫血,需要长期输血治疗。营养因素和寄生虫感染是铁缺乏的主要原因,铁缺乏情况很常见,尤其是在2岁以下的儿童中(87%)。东南亚裔患者的医生应了解这些血红蛋白病的临床和血液学表现。

相似文献

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Variable severity of Southeast Asian beta 0-thalassemia/Hb E disease.
Birth Defects Orig Artic Ser. 1987;23(5A):241-8.

本文引用的文献

1
Identification of hemoglobin E by the isopropanol solubility test.
Clin Biochem. 1980 Aug;13(4):146-8. doi: 10.1016/s0009-9120(80)91014-0.
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Clin Pediatr (Phila). 1982 Oct;21(10):613-6. doi: 10.1177/000992288202101010.
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Am J Dis Child. 1982 Aug;136(8):697-700. doi: 10.1001/archpedi.1982.03970440041011.
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