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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
Published on: August 15, 2019
Arthrogryposis, renal dysfunction, cholestasis syndrome with a novel mutation in two siblings
Rahiya Rehman1,2,3,4, Leslia Gonzalez1,3,4, Kelsey Kolbe3
1Department of Pediatrics Warren Alpert Medical School/Brown University Providence Rhode Island USA.
Abstract:
This current case series adds to the spectrum of Arthrogryposis renal dysfunction cholestasis (ARC)-associated variants. Increased awareness and early genetic testing for ARC are suggested in cases with failure to thrive, renal tubular dysfunction, and rickets, even when the degree of cholestasis is mild. Prompt identification and intervention may improve the quality of life.
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