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Autosomal Recessive Polycystic Kidney Disease—The Clinical Aspects and Diagnostic Challenges
Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common ciliopathies with kidney (nephromegaly, hypertension, renal dysfunction) and liver involvement (congenital hepatic fibrosis, dilated bile ducts). Clinical features also include growth failure and neurocognitive impairmen...
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| Publicado no: | J Pediatr Genet |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Georg Thieme Verlag KG
2021
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7853919/ https://ncbi.nlm.nih.gov/pubmed/33552631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0040-1714701 |
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