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Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease
Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phenotype often presenting prenatally or in early childhood. With its obligate renal and hepatic involvement, ARPKD is one of the most important indications for liver and/or kidney transplantation in chil...
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| Foilsithe in: | Front Pediatr |
|---|---|
| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Frontiers Media S.A.
2017
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5327862/ https://ncbi.nlm.nih.gov/pubmed/28296980 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2017.00018 |
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