Immunoglobulin M Nephropathy in a Patient with Wilson’s Disease

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Immunoglobulin M Nephropathy in a Patient with Wilson’s Disease

Immunoglobulin M nephropathy (IgMN) is characterized by the deposition of immunoglobulin M in a dominant distribution in the renal glomeruli. Primary immunoglobulin M nephropathy is diagnosed after consistent light microscopy (LM), immunofluorescence (IF), electron microscopy (EM) results, and exclusion of known systemic disorders causing immunoglobulin M deposition in the glomeruli. The second...

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Anesthetic Management of a Pediatric Patient With Wilsons Disease

UNLABELLED Wilsons disease, characterized by cirrhosis, extrapyramidal symptoms and Kayser-Fleischer corneal rings, is a rare hereditary disease of human copper metabolism. Clinical findings in Wilsons disease are complex and neurological symptoms such as tremor, dysarthria, rigid dystonia, seizures, psychiatric disorders, acute liver failure, chronic hepatitis or cirrhosis may develop. A 4-yea...

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anticardiolipin antibodies and immunoglobulin m and a in graves’ disease

background : graves’ disease is an autoimmune disease, characterized by the presence of antibodies directed to tsh receptor or nearby regions as well as antibodies to double strands dna (dsdna) anticardiolipin and nuclear antibodies. this study evaluated anticardiolipin and rheumatoid factor, such as iga and igm antibodies in patients with graves’ disease.   patients and methods: anticardiolipi...

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ژورنال

عنوان ژورنال: Cureus

سال: 2016

ISSN: 2168-8184

DOI: 10.7759/cureus.929