Dual diagnosis of autosomal dominant polycystic kidney disease and sickle cell disease in a teenage male

BACKGROUND: Sickle cell disease (SCD) and autosomal dominant polycystic kidney disease (ADPKD) are relatively common genetic conditions with considerable overlap in clinical presentation. In addition to similarities between the signs and symptoms in sickle cell nephropathy and ADPKD, more than half...

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Detalles Bibliográficos
Autores principales: Stein, Quinn, Herman, Kathleen, Deyo, Jennifer, McDonough, Colleen, Bloom, Michelle S., Mansuri, Asifhusen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432312/
https://www.ncbi.nlm.nih.gov/pubmed/36646975
http://dx.doi.org/10.1007/s00467-023-05873-6

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