摘要
马方综合征是一种常染色体显性遗传病,可引起心血管、眼、骨骼等多系统病变;系统性红斑狼疮与多基因遗传有关。二者同为结缔组织病,遗传基因及机制有无联系尚不明确,现汇报一例马方综合征合并系统性红斑狼疮患儿的临床表现,以供参考。
Marfan syndrome is an autosomal dominant genetic disease,which can cause cardiovascular,ocular,skeletal lesions.SLE is related to polygenic inheritance.Both diseases are connective tissue diseases.It is not clear whether their genetic genes and mechanisms overlap.The clinical manifestations of a child with Marfan syndrome complicated with systemic lupus erythematosus are reported for reference.
作者
刘玉洁
王向丽
江春亚
张书锋
刘翠华
LIU Yu-jie;WANG Xiang-Li;JIANG Chun-ya;ZHANG Shu-feng;LIU Cui-hua(Department of Renal rheumatology,Children's Hospital affiliated to Zhengzhou University(Henan Children's Hospital/Zhengzhou Children's Hospital),zhengzhou 450018,Henan province,china)
出处
《罕少疾病杂志》
2021年第1期3-4,共2页
Journal of Rare and Uncommon Diseases
关键词
马方综合征
系统性红斑狼疮
儿童
Marfan syndrome
Systemic lupus erythematosus
children