Foster M E, Foster D R
Postgrad Med J. 1980 Oct;56(660):718-9. doi: 10.1136/pgmj.56.660.718.
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.
马凡氏综合征是一种罕见的遗传性疾病,其特征为骨骼、心血管和眼部异常。约10%的患者会出现肺部异常,最常见的是自发性气胸和肺气肿。本文描述了一名患有马凡氏综合征和支气管扩张症的患者,这种关联在以往文献中仅被提及过两次。