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PAX2 Mutation-Related Oligomeganephronia in a Young Adult Patient
Oligomeganephronic hypoplasia, commonly referred to as oligomeganephronia (OMN), is a rare pediatric disorder characterized by small kidneys. Histologically a paucity of nephrons is observed which show compensatory enlargement. Hyperfiltration injury leads to end-stage kidney disease. Here we report...
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| Vydáno v: | Case Rep Nephrol Dial |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
S. Karger AG
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7747074/ https://ncbi.nlm.nih.gov/pubmed/33363218 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000510841 |
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