Primary ciliary dyskinesia

B. Rubbo, M. Goutaki, J. Lucas
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Abstract

● ● The European Respiratory Society (ERS) Task Force Guidelines for diagnosing PCD recommend that patients should be referred for diagnostic testing if they have several of the following features: persistent wet cough; situs anomalies; congenital cardiac defects; persistent rhinitis; chronic middle ear disease with or without hearing loss; or a history, in term infants, of neonatal upper and lower respiratory symptoms or neonatal intensive care admission.
原发性纤毛运动障碍
●●欧洲呼吸学会(ERS)诊断PCD的工作组指南建议,如果患者有以下几个特征,应转诊进行诊断测试:持续湿咳;位置异常;先天性心脏缺陷;持续的鼻炎;伴有或不伴有听力损失的慢性中耳疾病;或足月婴儿有新生儿上呼吸道和下呼吸道症状史或新生儿重症监护史。
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