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- John Morgan, Michael A Sadler, and Stacey Siegel.
- Department of Radiology, St. Vincent's Hospital and Medical Center, New York, NY 10011, USA. jmorgan911@aol.com
- Clin Imaging. 2008 Sep 1; 32 (5): 393-5.
AbstractAlström syndrome is among the rarest genetic disorders described in the medical literature. It is characterized by retinal pigment degeneration, obesity, sensorineural deafness, non-insulin-dependent diabetes mellitus, progressive chronic nephropathy, cardiomyopathy, and hepatic dysfunction. Hepatic inflammation and fibrosis, which leads to cirrhosis, portal hypertension, and liver failure, is the final pathway of the hepatopathy in Alström syndrome. We report a case of Alström syndrome with particular emphasis on hepatic findings.
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