卡塔赫纳综合征1例报告。

Q3 Medicine

Ethiopian Medical Journal Pub Date : 2016-04-01

Samuel Sisay Hailu, Eyoel Degafu Amerga, Yocabel Gorfu, Daniel Zewedneh

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引用次数: 0

摘要

卡塔格纳氏综合征是一种罕见的常染色体隐性遗传疾病，它会导致呼吸道纤毛的功能缺陷。患者通常表现为由假单胞菌感染引起的慢性复发性鼻窦炎、中耳炎、肺炎和支气管扩张。在本病例报告中，我们报告了一名来自Tikur Anbessa教学医院的12岁女性Kartagener综合征，据我们所知，这是埃塞俄比亚第一例此类病例。讨论了临床和影像学表现。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

本刊更多论文

KARTAGENER'S SYNDROME: A CASE REPORT.

Kartagener's syndrome is a rare autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract. Patients usually present with chronic recurrent rhinosinusitis, otitis media, pneumonia, and bronchiectasis caused by Pseudomonas infection. In this case report, we present a 12-year old female with Kartagener's syndrome from Tikur Anbessa Teaching Hospital which to our knowledge is the first of it's kind to be reported in Ethiopia. The clinical and imaging findings are discussed.

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来源期刊

Ethiopian Medical Journal Medicine-Medicine (all)

CiteScore

0.40

自引率

0.00%

发文量

期刊介绍： The Ethiopian Medical Journal (EMJ) is the official Journal of the Ethiopian Medical Association (EMA) and devoted to the advancement and dissemination of knowledge pertaining to the broad field of medicine in Ethiopia and other developing countries. Prospective contributors to the Journal should take note of the instructions of Manuscript preparation and submission to EMJ as outlined below.