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Other Sphingolipidosis

MedGen UID:
1826267
•Concept ID:
C0348489
•
Disease or Syndrome

Definition

Evidence of other sphingolipidosis not specified elsewhere. [from NCI]

Professional guidelines

PubMed

Fabry Disease: The Current Treatment Landscape.
Lenders M, Brand E
Drugs 2021 Apr;81(6):635-645. Epub 2021 Mar 15 doi: 10.1007/s40265-021-01486-1. PMID: 33721270Free PMC Article
Treatment of Anderson-Fabry Disease.
Simonetta I, Tuttolomondo A, Daidone M, Miceli S, Pinto A
Curr Pharm Des 2020;26(40):5089-5099. doi: 10.2174/1381612826666200317142412. PMID: 32183665
Developments in the treatment of Fabry disease.
van der Veen SJ, Hollak CEM, van Kuilenburg ABP, Langeveld M
J Inherit Metab Dis 2020 Sep;43(5):908-921. Epub 2020 Mar 2 doi: 10.1002/jimd.12228. PMID: 32083331Free PMC Article

Recent clinical studies

Prognosis

The incidence rate of hospitalized lysosomal storage diseases in Poland in 2013-2015 based on data from the National Health Fund.
Grzeszczak W, Franek E, Szypowska A, Filipow W, Zięba M, Kabicz P, Więckowska B
Pediatr Endocrinol Diabetes Metab 2021;27(3):191-198. doi: 10.5114/pedm.2021.107715. PMID: 34498441Free PMC Article

Supplemental Content

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    Practice guidelines

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