[Primary ciliary dyskinesia in children]
نویسندگان
چکیده
OBJECTIVES: To point out primary ciliary dyskinesia as a cause of chronic respiratory disease in children.METHODS: A 10 year literature review on Medline and by direct research about the subject.RESULTS AND CONCLUSIONS: Primary ciliary dyskinesia is a disorder characterized by an abnormal mucociliary clearance. It affects both the upper and lower respiratory tracts and usually the clinical manifestations start in the first years of life. It can progress to bronchiectasis. Kartageners syndrome is the typical genetic manifestation. The diagnosis may be based on an abnormal saccharin test, but its confirmation depends on abnormal ultrastructure of the cilia or abnormal ciliary function. Many ciliary defects are currently known. The treatment is supportive, with measures to enhance mucociliary clearance, such as chest physiotherapy, prevention of infections by immunizations and prompt antibiotic therapy in the acute respiratory infections.
منابع مشابه
گزارش دو مورد اختلال حرکت اولیه مژک ها (گزارش مورد)
Primary ciliary dyskinesia and Kartagener's syndrome are rare genetic disorders. There is a ciliary dysfunction in these disorders that cause recurrent infections in respiratory and sinus tracts associated with dextrocardia, chronic vasomotor rhinitis and dextrocardia. The aim of this paper is to report two rare cases of Primary ciliary dyskinesia, including one case of primary ciliary dyskin...
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1 Bush A, Chodhari R, Collins N, et al. Primary ciliary dyskinesia: current state of the art. Arch Dis Child 2007; 92: 1136–1140. 2 Lie H, Ferkol T. Primary ciliary dyskinesia: recent advances in pathogenesis, diagnosis and treatment. Drugs 2007; 67: 1883–1892. 3 Pifferi M, Cangiotti AM, Ragazzo V, et al. Primary ciliary dyskinesia: diagnosis in children with inconclusive ultrastructural evalua...
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ورودعنوان ژورنال:
- Jornal de pediatria
دوره 76 1 شماره
صفحات -
تاریخ انتشار 2000