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Proteinuric glomerulopathy in an adolescent with a distal partial trisomy chromosome 1
We report a case of distal partial trisomy 1 from q32.1 to 41 that have exhibited proteinuric glomerulopathy. The patient was a 17-year-old adolescent with clinical features of low birth weight, mild mental retardation and mild deafness, from the birth. He exhibited non-nephrotic range proteinuria w...
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| Vydáno v: | CEN Case Rep |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Japan
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6181882/ https://ncbi.nlm.nih.gov/pubmed/29766469 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-018-0337-y |
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