期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
Milroy Disease:A Case Report
1
作者 Goncalo Gomes Pereira Joana Moreira +1 位作者 Vaz de Macedo Mário Santos 《Case Reports in Clinical Medicine》 2015年第11期349-351,共3页
Hereditary lymphoedema type I is a congenital onset primary lymphoedema with autosomal dominant inheritance, which is characterized by the swelling of the lower body. In this article, the authors report a case of a 32... Hereditary lymphoedema type I is a congenital onset primary lymphoedema with autosomal dominant inheritance, which is characterized by the swelling of the lower body. In this article, the authors report a case of a 32-year-old woman with repeating episodes of swollen limbs. Imaging studies and genetic study were carried out and a Milroy’s syndrome diagnosis was established. The patient started sintomatic treatment of the edema, with fitting stockings and descompressive massage, with symptomatic benefit. 展开更多
关键词 milroy Disease Lower Limbs Edema FLT4 Gene VEGFR-3
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部