A rare non-syndromic urogenital tract malformation with the familial occurrence of retrograde flow of urine from the bladder into the ureter and sometimes the kidneys. Patients may be asymptomatic or may present with recurrent, sometimes febrile, uri

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reflux vésico-urétéral familial

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This syndrome has characteristics of the association of acanthosis nigricans, insulin resistance, severe muscle cramps and acral hypertrophy. At least five cases have been described in the literature so far. Enlargement of the kidneys was also report

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syndrome d'acanthosis nigricans-résistance à l'insuline-crampes-hypertrophie acrale

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A rare subtype of renal cell carcinoma, occurring in the context of end-stage kidney disease and acquired cystic kidney disease, characterized by a usually well circumscribed, solid, multifocal, bilateral tumor with inter or intracellular micro lumen

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carcinome rénal associé à une maladie kystique acquise

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The Kidney Foundation of Canada

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La Fondation canadienne du rein [ Fondation canadienne des maladies du rein ]

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Date index: 2021-07-23