Homozygous hemoglobin Lepore disease in a child: A case report

Rimjhim Sonowal , Aditi Das , Atanu Kumar Dutta , Nihar Ranjan Mishra
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引用次数: 0

Abstract

Background

Hemoglobin Lepore is a rare variant of structurally abnormal hemoglobin. Homozygous hemoglobin Lepore is even more rare.

Case report

We describe a case of homozygous hemoglobin Lepore in a 4-year 8-month-old boy. He presented with a thalassemia intermedia-like presentation. His diagnosis was confirmed by family screening with high-performance liquid chromatography (HPLC) and genetic testing.

Conclusion

Homozygous hemoglobin Lepore can present as thalassemia intermedia. It can be a diagnostic dilemma if only patient's HPLC is reported. Genetic testing and family screening aid to identify and confirm this uncommon variant of hemoglobin.

儿童同型血红蛋白莱波尔病:病例报告
背景血红蛋白列波尔是一种罕见的结构异常血红蛋白变异体。病例报告我们描述了一例 4 岁 8 个月大的同型血红蛋白勒波尔男孩。他表现为类似地中海贫血的症状。通过使用高效液相色谱(HPLC)进行家族筛查和基因检测,他的诊断得到了证实。如果只报告患者的高效液相色谱,可能会造成诊断难题。基因检测和家族筛查有助于识别和确认这种不常见的血红蛋白变异。
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