Coleman R A, Van Hove J L, Morris C R, Rhoads J M, Summar M L
Department of Nutrition, University of North Carolina at Chapel Hill 27599, USA.
Am J Med Genet. 1997 Oct 31;72(3):335-8.
We report on 4 children from 2 unrelated families who appear to have the lethal ARC syndrome (arthrogryposis, renal tubular dysfunction, and cholestasis) together with the additional findings of nephrogenic diabetes insipidus and cerebral anomalies, including deafness. With increased survival time in our patients, paucity of the intrahepatic bile ductules and cholestasis progressed to cirrhosis, growth was severely impaired, and severe mental retardation became apparent. No evidence was found for peroxisomal, chromosomal, or mitochondrial disorders. We propose to amend the ARC mnemonic to ARCC-NDI (A-Arthrogryposis, R-renal Fanconi, C-cerebral, C-cholestasis, NDI-nephrogenic diabetes insipidus) to name the major manifestations of this syndrome, several of which have not been appreciated.
我们报告了来自两个无血缘关系家庭的4名儿童,他们似乎患有致死性的ARC综合征(关节挛缩、肾小管功能障碍和胆汁淤积),并伴有肾性尿崩症和脑异常等其他表现,包括耳聋。随着我们患者存活时间的延长,肝内胆小管稀少和胆汁淤积发展为肝硬化,生长严重受损,严重智力发育迟缓变得明显。未发现过氧化物酶体、染色体或线粒体疾病的证据。我们建议将ARC记忆法修改为ARCC-NDI(A-关节挛缩,R-肾性范科尼综合征,C-脑,C-胆汁淤积,NDI-肾性尿崩症),以命名该综合征的主要表现,其中一些表现此前未被认识到。