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Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations
BACKGROUND: Congenital nephrotic syndrome (CNS) is a rare disorder caused by various structural and developmental defects of glomeruli. It occurs typically as an isolated kidney disorder but associates sometimes with other systemic, extrarenal manifestations. CASE PRESENTATIONS: An infant presented...
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| 發表在: | BMC Nephrol |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5501564/ https://ncbi.nlm.nih.gov/pubmed/28683731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-017-0632-4 |
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