Patients With Infantile Nephropathic Cystinosis in Germany and Austria: A Retrospective Cohort Study

BACKGROUND: Infantile nephropathic cystinosis (INC) is a rare lysosomal storage disorder resulting in progressive chronic kidney disease (CKD) and a variety of extrarenal manifestations. This orphan disease remains a challenge for patients, their families and health care providers. There is currentl...

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Detalles Bibliográficos
Autores principales: O'Connell, Nina, Oh, Jun, Arbeiter, Klaus, Büscher, Anja, Haffner, Dieter, Kaufeld, Jessica, Kurschat, Christine, Mache, Christoph, Müller, Dominik, Patzer, Ludwig, Weber, Lutz T., Tönshoff, Burkhard, Weitz, Marcus, Hohenfellner, Katharina, Pape, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082678/
https://www.ncbi.nlm.nih.gov/pubmed/35547226
http://dx.doi.org/10.3389/fmed.2022.864554

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082678/
https://www.ncbi.nlm.nih.gov/pubmed/35547226
http://dx.doi.org/10.3389/fmed.2022.864554

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