| Literature DB >> 34227055 |
Takuto Torimitsu1, Tadashi Yoshida2, Satomi Nishi3, Hiroshi Itoh1, Mototsugu Oya4,5.
Abstract
Alström syndrome (AS) is an extremely rare disease accompanied by blindness, hearing loss, obesity, type 2 diabetes, dilated cardiomyopathy, and progressive hepatic and renal dysfunction. The life span of AS patients rarely exceeds 50 years, and thus there are very few reports describing the implementation of renal replacement therapy for these patients. We here report a case of AS patient who exhibited dilated cardiomyopathy, end-stage renal disease, and hepatic cirrhosis. He underwent hemodialysis therapy more than 3 years. Although he eventually died of amiodarone-induced multiple organ damage in the lungs and liver, the present case suggests that hemodialysis therapy can be a choice of renal replacement therapy for AS patients with end-stage renal disease.Entities:
Keywords: Amiodarone; End-stage renal disease; Hepatic cirrhosis; Hereditary kidney disease
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Year: 2021 PMID: 34227055 PMCID: PMC8811015 DOI: 10.1007/s13730-021-00621-x
Source DB: PubMed Journal: CEN Case Rep ISSN: 2192-4449