Cortical microcystic disease of the kidney with dominant inheritance: a previously undescribed syndrome.
We report a family in which the father and all three children had symptomless chronic renal failure and, in the case of the children, normocytic, normochromic anaemia. None had hypertension, proteinuria, or abnormality of urinary deposit. Renal biopsy specimens showed microcysts confined to the rena...
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| Publicado no: | J Clin Pathol |
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| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1984
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC498767/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6725594/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jcp.37.5.494 |
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