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首页> 外文期刊>The Turkish journal of pediatrics. >A rare cause of acute abdominal pain in a patient with primary ciliary dyskinesia with situs inversus totalis
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A rare cause of acute abdominal pain in a patient with primary ciliary dyskinesia with situs inversus totalis

机译：患有原发性逆血管患者患者患者急性腹痛的罕见原因

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Primary ciliary dyskinesia (PCD) is a rare, genetic disease characterized by ciliary dysfunction. Patients may present with respiratory distress during neonatal period; chronic sinopulmonary disease, bronchiectasis, recurrent otitis media, sinusitis and infertility in later periods. About 50% of PCD patients have situs inversus totalis and 6-12% have situs ambiguous known as heterotaxy syndromes. Herein, we present a case of PCD and accompanying situs inversus who had acute abdominal pain and was diagnosed with torsion of one of the multiple spleens. Evaluation of acute abdominal pain in these patients has great importance since the internal organs are not at their typical locations.
机译：原发性睫状剂量障碍（PCD）是一种罕见的遗传症，其特征在于睫状体功能障碍。患者在新生儿期间可能存在呼吸窘迫;慢性肺尿疾病，支气管扩张，经常发生的中耳炎，鼻窦炎和后期不孕症。大约50％的PCD患者的SITUS Inversus TOMITIS和6-12％的SITUS含糊不清，称为异也综合征。在此，我们提出了PCD的情况，并伴随着患有急性腹痛的SITUS逆变，并被诊断出患有多个脾脏中的一种扭转。这些患者中急性腹痛的评估具有很大的重要性，因为内脏不在其典型地点。

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