马凡氏综合征是一种先天性发育不正常疾病,其主要表现为眼一骨骼—心血管三联征。多数病人以眼病求诊于眼科,故内科对本病报道较少。我院曾见3例,其中1例曾以气喘心衰多次住院而第三次住院才确诊为本病,说明本病并非少见。例1 朱××,女,60岁,农民。因心悸、气促5年于1976年入院。患者1971年起反复心悸、气喘,活动时尤甚。双 Marfan syndrome is a congenital anomalous development of the disease, which is mainly manifested as a skeleton-cardiovascular triad. The majority of patients treated with ophthalmology in ophthalmology, so less medical reports of the disease. 3 cases have been seen in our hospital, of which 1 case had multiple hospitalizations with asthma and heart failure, the third hospital was diagnosed as the disease, indicating that the disease is not uncommon. Example 1 Zhu × ×, female, 60 years old, farmer. Due to heart palpitations, shortness of breath 5 years admitted to hospital in 1976. Patients from 1971 repeated palpitations, asthma, especially in activities. double