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马凡氏综合征(Marfan’s Syndrome)是一种累及骨骼、眼和心脏大血管为主的结缔组织代谢障碍的遗传性疾病,我院近收治1例合并肾炎报告如下: 病例报告患儿关××,女,13岁,广东人,住院号61267,因浮肿尿少5天于1980年8月入院。患儿于半月前左足有一(疒节)肿,入院前5天出现浮肿,从颜面开始下行发展至全身,伴尿少。无肉眼血尿、尿频、头痛、心悸、咳嗽、气促及发热等症状。自幼体型细长瘦弱。头颅、颜面、胸廓、指趾均有畸形。因高度近视未能
Marfan’s Syndrome (Marfan’s Syndrome) is a genetic disease involving the metabolic disorders of the connective tissue dominated by bone, eyes and heart blood vessels. One case of nephritis with recent treatment in our hospital is reported as follows: , Female, 13 years old, Cantonese, hospital number 61267, less than 5 days due to edema in August 1980 admitted. Children with a left foot (tuberosity) swollen half a month ago, five days before admission edema, down from the face to the development of the body, with less urine. No gross hematuria, frequent urination, headache, palpitations, cough, shortness of breath and fever and other symptoms. Slim and thin since childhood. Head, face, thorax, toe deformity. Due to a high degree of myopia failed