Art
J-GLOBAL ID:202002244296965687   Reference number:20A2182552

Late-onset Fabry Disease Diagnosed by the Detection of Urinary Mulberry Cells during Medical Check-up

人間ドックにおける尿中マルベリー細胞の検出を契機に遅発型Fabry病の確定診断に至った一症例
Author (12):
Material:
Volume: 35  Issue:Page: 210-216  Publication year: Sep. 30, 2020 
JST Material Number: L0494A  ISSN: 1880-1021  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Category name(code) classified by JST.
Diagnostics of congenital diseases, deformities. 
Reference (19):
  • 1)Fabry J: Ein Beitrag Zur Kenntnis der Purpura haemorrhagica nodulatis(Purpura papulosa hemorrhagica Hebrae). Arch Dermatol Syph 1898; 43: 187-200.
  • 2)Anderson W: A case of angiokeratom. Br J Dermatol 1898; 10: 113-117.
  • 3)National Institute of Health, U.S. Department of Health & Human Services: Genetics Home Reference. https://ghr.nlm.nih.gov/gene/GLA#location[2020.1.9]
  • 4)Saito S, Ohno K, Sakuraba H: Fabry-database.org, last updated Feb. 15, 2019. http://fabry-database.org/mutants/[2020.1.9]
  • 5)Desnick RJ, Banikazemi M, Wasserstein M: Enzyme replacement therapy for Fabry disease, an inherited nephropathy. Clin Nephrol 2002; 57: 1-8.
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