Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis syndrome.
作者信息
Saraiva J M, Mota H C
出版信息
J Med Genet. 1994 Oct;31(10):820. doi: 10.1136/jmg.31.10.820-a.
Abstract
摘要
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本文引用的文献
1
Liver histology in the arthrogryposis multiplex congenita, renal dysfunction, and cholestasis (ARC) syndrome: report of three new cases and review.先天性多发性关节挛缩症、肾功能不全和胆汁淤积（ARC）综合征的肝脏组织学：三例新病例报告及文献复习
J Med Genet. 1994 Jan;31(1):62-4. doi: 10.1136/jmg.31.1.62.
2
Renal tubular insufficiency, cholestatic jaundice, and multiple congenital anomalies--a new multisystem syndrome.肾小管功能不全、胆汁淤积性黄疸和多种先天性异常——一种新的多系统综合征。
Helv Paediatr Acta. 1984 Dec;39(5-6):463-71.
3
Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: report of a second family.
Am J Med Genet. 1990 Oct;37(2):237-40. doi: 10.1002/ajmg.1320370214.
4
Arthrogryposis multiplex congenita with renal and hepatic abnormalities in a female infant.一名患有先天性多发性关节挛缩症并伴有肾脏和肝脏异常的女婴。
J Pediatr. 1990 Nov;117(5):761-3. doi: 10.1016/s0022-3476(05)83339-6.
5
A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease.一种致命的家族性综合征，合并先天性多发性关节挛缩、肾功能不全以及胆汁淤积性和色素沉着性肝病。
J Pediatr. 1979 Feb;94(2):258-60. doi: 10.1016/s0022-3476(79)80839-2.
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