Bronchiectasis and Marfan's syndrome.
نویسندگان
چکیده
Marfan's syndrome is a rare hereditary disorder characterized by skeletal, cardiovascular and ocular abnormalities. Pulmonary abnormalities occur in approximately 10% of patients the commonest being spontaneous pneumothorax and emphysema. A patient is described who had Marfan's syndrome and bronchiectasis, an association only described on 2 previous occasions in the literature.
منابع مشابه
Aortic Root Dilatation and Mitral Valve Prolapse in Marfan's Syndrome
Echocardiographic and phonocardiographic findings in 35 patients with Marfan's Syndrome and ten patients without Marfan's or other clinically apparent connective tissue disorders but with angiographic and echocardiographic evidence of mitral prolapse are reported and compared. Echocardiography revealed aortic root dilatation and/or mitral valve prolapse in 97% of the patients with Marfan's Synd...
متن کاملAortic root dilatation and mitral valve prolapse in Marfan's syndrome: an ECHOCARDIOgraphic study.
Echocardiographic and phonocardiographic findings in 35 patients with Marfan's Syndrome and ten patients without Marfan's or other clinically apparent connective tissue disorders but with angiographic and echocardiographic evidence of mitral prolapse are reported and compared. Echocardiography revealed aortic root dilatation and/or mitral valve prolapse in 97% of the patients with Marfan's Synd...
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AIM To examine evolution of the physical characteristics of Marfan's syndrome throughout childhood. METHODS 40 children were ascertained during the development of a regional register for Marfan's syndrome. Evolution of the clinical characteristics was determined by repeat evaluation of 10 patients with sporadic Marfan's syndrome and 30 with a family history of the condition. DNA marker studie...
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Various pulmonary problems have been described in Marfan's syndrome. Unusual cystic lung changes in a young girl with Marfan's syndrome are described.
متن کاملThe prevalence of obstructive sleep apnoea and its association with aortic dilatation in Marfan's syndrome.
BACKGROUND Craniofacial abnormalities and increased pharyngeal collapsibility due to abnormal connective tissue suggest the possibility of an increased prevalence of obstructive sleep apnoea (OSA) in patients with Marfan's syndrome but the actual prevalence is uncertain. Aortic dilatation and dissection are life threatening manifestations of Marfan's syndrome and case reports have suggested a p...
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ورودعنوان ژورنال:
- Postgraduate medical journal
دوره 56 660 شماره
صفحات -
تاریخ انتشار 1980