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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Melnick, S C, Brewer, D B, Oldham, J S
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1984
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC498767/
https://ncbi.nlm.nih.gov/pubmed/6725594
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