Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome: from molecular genetics to clinical features

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Term Occurence Count Dictionary
Fanconi syndrome 1 nephrologydiseases
nephrogenic diabetes insipidus 1 nephrologydiseases
renal tubular acidosis 4 nephrologydiseases

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Fanconi syndrome 9174 dysfunction, and cholestasis.Renal tubular dysfunctionRenal tubular dysfunction manifests in the form of Fanconi syndrome , with symptoms including renal tubular acidosis, nephrogenic diabetes insipidus, glucosuria, aminoaciduria,
nephrogenic diabetes insipidus 9240 dysfunction manifests in the form of Fanconi syndrome, with symptoms including renal tubular acidosis, nephrogenic diabetes insipidus , glucosuria, aminoaciduria, and phosphaturia [[19],[20]]. During episodes of intercurrent illness, renal
renal tubular acidosis 3152 liver, and central nervous at birth. The characteristic features of ARC syndrome include arthrogryposis, renal tubular acidosis , and neonatal cholestatic jaundice (see Figure 1) [[2]]. These features are sometimes accompanied by
renal tubular acidosis 9216 dysfunctionRenal tubular dysfunction manifests in the form of Fanconi syndrome, with symptoms including renal tubular acidosis , nephrogenic diabetes insipidus, glucosuria, aminoaciduria, and phosphaturia [[19],[20]]. During episodes
renal tubular acidosis 9370 insipidus, glucosuria, aminoaciduria, and phosphaturia [[19],[20]]. During episodes of intercurrent illness, renal tubular acidosis may be notably exacerbated, which is symptomatic of renal tubular calcification and degeneration. Renal
renal tubular acidosis 20433 clinical diagnosis of ARC syndrome consists of identifying the triad conditions of arthrogryposis, renal tubular acidosis , and neonatal cholestatic jaundice with low γGT activity, combined with pathologic confirmation. However,

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