Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: Report of a second family
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference3 articles.
1. A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease
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1. A 45-Day-Old Infant: A Case Report of Arthrogryposis-Renal Dysfunction-Cholestasis (ARC) Syndrome;Nephro-Urology Monthly;2019-06-08
2. Le phénotype complexe du syndrome ARC : une nouvelle observation;Archives de Pédiatrie;2017-02
3. Liver Transplant in a Case of Arthrogryposis-Renal Tubular Dysfunction-Cholestasis Syndrome With Severe Intractable Pruritus;Experimental and Clinical Transplantation;2013-06-17
4. Arthrogryposes (Multiple Congenital Contractures);Emery and Rimoin's Principles and Practice of Medical Genetics;2013
5. Orthopaedic Manifestations of Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome;Journal of Pediatric Orthopaedics;2011-01
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