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The retinal phenotype in primary hyperoxaluria type 2 and 3

BACKGROUND: The primary hyperoxalurias (PH1-3) are rare inherited disorders of the glyoxylate metabolism characterized by endogenous overproduction of oxalate. As oxalate cannot be metabolized by humans, oxalate deposits may affect various organs, primarily the kidneys, bones, heart, and eyes. Visio...

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Detalles Bibliográficos
Autores principales:	Birtel, Johannes, Diederen, Roselie M., Herrmann, Philipp, Kaspar, Sophie, Beck, Bodo B., Garrelfs, Sander F., Hoppe, Bernd, Charbel Issa, Peter
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060347/ https://www.ncbi.nlm.nih.gov/pubmed/36260161 http://dx.doi.org/10.1007/s00467-022-05765-1

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