Clinical Characteristics, Renal Involvement, and Therapeutic Options of Pediatric Patients With Fabry Disease

• Hauptverfasser: Carmen Muntean (Verfasst von), Iuliana Magdalena Starcea (Verfasst von), Cristina Stoica (Verfasst von), Claudia Banescu (Verfasst von)
• Format: Buch
• Veröffentlicht: Frontiers Media S.A., 2022-06-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: Connect to this object online.

Inherited renal diseases represent 20% of the causes of end-stage renal diseases. Fabry disease, an X-linked lysosomal storage disorder, results from α-galactosidase A deficient or absent activity followed by globotriaosylceramide (Gb3) accumulation and multiorgan involvement. In Fabry disease, kidn...