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Tuberous sclerosis complex with autosomal dominant polycystic kidney disease: a rare duo
Tuberous sclerosis complex (TSC) is an autosomal dominant condition characterised by the presence of multiple hamartomas in various organ systems in the body. The kidneys are affected in 80% of patients, usually in the form of renal angiomyolipomas, renal cysts or renal cell carcinoma. Although extr...
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| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4275747/ https://ncbi.nlm.nih.gov/pubmed/25519866 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2014-207471 |
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