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Congenital solitary kidney in autosomal dominant polycystic kidney disease: Where do known genes end and the unknown begin?
We present the case of a 41‐year‐old man patient diagnosed with solitary left kidney with few cysts. He has a family history of unilateral renal agenesis (URA) but no for autosomal dominant polycystic kidney disease (ADPKD). Genetic testing revealed PKD1 gene intron 11 heterozygous nucleotide varian...
Autores principales: | Bucci, Romina, Tunesi, Francesca, De Rosa, Liliana Italia, Carrera, Paola, Mancassola, Giulia, Catania, Martina, Vezzoli, Giuseppe, Sciarrone Alibrandi, Maria Teresa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10663533/ https://www.ncbi.nlm.nih.gov/pubmed/38028110 http://dx.doi.org/10.1002/ccr3.7917 |
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