东氏综合征的血液学诊断及文献复习

S. Raj, D. Aden
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引用次数: 0

摘要

Chediak Higashi综合征是一种罕见的常染色体隐性遗传病,发病早,多见于儿科,具有致命性。在印度,直到2000年,只报告了5例。在这项研究中,我们介绍了在印度报告的所有病例,他们的临床表现、CBC、PBS、骨髓结果、皮肤活检或头发研究(如果进行)以及它们之间的相关性,以了解疾病的加速阶段和治疗方法。在印度等发展中国家,确定外周血涂片检查是诊断Chediak Higashi综合征的关键,它是我国最简单、最快捷、最便宜、最容易获得的检查方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chédiak Higashi Syndrome -A hematological Diagnosis and Review of Literature
Chediak Higashi Syndrome is a rare autosomal recessive disease come in picture early in age, mainly paediatric group and is fatal. In India, till the year 2000, only five cases have been reported. In this study ,we present all the cases reported in India, their clinical presentation, CBC ,PBS ,Bone marrow findings, skin biopsy or hair study (if performed) and their correlation to see the accelerated phase of the disease and approach to the management. Determined peripheral blood smear examination is the key to arrest the diagnosis of Chediak Higashi Syndrome in developing country like India, defining it is the most easiest, quickest, cheap, easily available investigation in our country.
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