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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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Detalhes bibliográficos
Publicado no:J Clin Pathol
Principais autores: Melnick, S C, Brewer, D B, Oldham, J S
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 1984
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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