Cargando…
An Adult Patient with Alagille Syndrome Showing Mainly Renal Failure and Vascular Abnormality without Liver Manifestation
Alagille syndrome is an inherited multisystemic disorder. We herein report an atypical case of a Japanese adult patient with Alagille syndrome. He had been diagnosed with Alagille syndrome as an infant based on a liver biopsy. At 27 years of age, he needed to start hemodialysis therapy, but an arter...
Autores principales: | Shimohata, Homare, Imagawa, Kazuo, Yamashita, Marina, Ohgi, Kentaro, Maruyama, Hiroshi, Takayasu, Mamiko, Hirayama, Kouichi, Kobayashi, Masaki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725619/ https://www.ncbi.nlm.nih.gov/pubmed/32727995 http://dx.doi.org/10.2169/internalmedicine.4780-20 |
Ejemplares similares
-
A Case of Proliferative Glomerulonephritis with Monoclonal IgG Deposits That Showed Predominantly Membranous Features
por: Shimohata, Homare, et al.
Publicado: (2017) -
Serum 20S proteasome levels are associated with disease activity in MPO-ANCA-associated microscopic polyangiitis
por: Maruyama, Hiroshi, et al.
Publicado: (2020) -
Microscopic polyangiitis associated with thymic tumor: a case report and review of the literature
por: Miyamoto, Yasunori, et al.
Publicado: (2019) -
Staphylococcus aureus Infection-Related Glomerulonephritis with Dominant IgA Deposition
por: Takayasu, Mamiko, et al.
Publicado: (2022) -
A Renal Variant of Fabry Disease Diagnosed by the Presence of Urinary Mulberry Cells
por: Shimohata, Homare, et al.
Publicado: (2016)