Fabry disease – a genetically conditioned extremely rare disease with a very unusual course
Author:
Affiliation:
1. Department of Internal Medicine, Diabetology and Nephrology, Medical University of Silesia, Katowice, Poland.
Publisher
International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/irdr/11/1/11_2021.01132/_pdf
Reference8 articles.
1. 1. Fabry J. "Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)". Archiv für Dermatologie und Syphilis. 1898; 43:187-200. doi:10.1007/bf01986897. ISSN 0340-3696. S2CID 33956139. (in German)
2. 2. Anderson W. A Case of "Angeio-Keratoma". Br J Dermatol. 1898; 10:113-117.
3. 3. Chimenti C, Scopelliti F, Vulpis E, Tafani M, Villanova L, Verardo R, De Paulis R, Russo MA, Frustaci A. Increased oxidative stress contributes to cardiomyocyte dysfunction and death in patients with Fabry disease cardiomyopathy. Hum Pathol. 2015; 46:1760-1768.
4. 4. Rozenfeld PA, de Los Angeles Bolla M, Quieto P, Pisani A, Feriozzi S, Neuman P, Bondar C. Pathogenesis of Fabry nephropathy: The pathways leading to fibrosis. Mol Genet Metab. 2020; 129:132-141.
5. 5. McGovern MM, Desnick RJ. Lysosomal storage diseases. Cecil Textbook of Medicine. In: Goldman L, editor. 21st ed. St. Louis: W.B. Saunders Company; 2000. pp.1104-1107.
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