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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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| 出版年: | J Pediatr Genet |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Georg Thieme Verlag KG
2021
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| オンライン･アクセス: | 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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