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A case of lipoprotein glomerulopathy with a rare apolipoprotein E isoform combined with neurofibromatosis type I
Lipoprotein glomerulopathy (LPG) is a rare inherited disease characterized by histopathological features of lipoprotein thrombi in dilated glomerular capillaries and type III like hyperlipoproteinemia with heterozygous mutation of the apolipoprotein (apo) E gene. We herein present the case of a 50-y...
Gorde:
| Argitaratua izan da: | CEN Case Rep |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer Japan
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886940/ https://ncbi.nlm.nih.gov/pubmed/29356944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-018-0309-2 |
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