Long-term Follow Up of a Boy with Unilateral Autosomal Dominant Polycystic Kidney Disease and Contralateral Renal Agenesis

In patients with autosomal dominant polycystic kidney disease (ADPKD) coexisting abnormalities of the urinary tract are considered rare. Only a few patients with ADPKD and congenital abnormalities of the kidney and urinary tract- renal agenesis, hypoplasia, aplasia, horseshoe kidney, ectopic multicy...

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Detalles Bibliográficos
Autores principales: Krzemień, Grażyna, Turczyn, Agnieszka, Pańczyk-Tomaszewska, Małgorzata, Jakimów-Kostrzewa, Aleksandra, Szmigielska, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2018
Materias:
Original articles/Prace oryginalne
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522938/
https://www.ncbi.nlm.nih.gov/pubmed/29291365
http://dx.doi.org/10.34763/devperiodmed.20172104.380383

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522938/
https://www.ncbi.nlm.nih.gov/pubmed/29291365
http://dx.doi.org/10.34763/devperiodmed.20172104.380383

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