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Significados de congenital biliary ectasias em inglês

russo
поликистоз почек
português
doença do rim policístico
catalão
poliquistosi renal
espanhol
poliquistosis renal

Congenital disorder of urinary system.

        doença do rim policístico
        Sinônimos
        Examples for "autosomal dominant polycystic kidney disease"
        Examples for "autosomal dominant polycystic kidney disease"
        1
        Cerebral aneurysms are sometimes associated with inherited diseases like autosomal dominant polycystic kidney disease.
        Pubmed
        2
        An intriguing feature of autosomal dominant polycystic kidney disease (ADPKD) is the focal and sporadic nature of individual cyst formation.
        Pubmed
        3
        In light of the parallels between cancer and autosomal dominant polycystic kidney disease (ADPKD), the latter is currently being studied as a metabolic disease.
        Pubmed
        4
        The rate at which autosomal dominant polycystic kidney disease (ADPKD) progresses to end-stage renal disease varies widely and is determined by genetic and non-genetic factors.
        Pubmed
        5
        Background and purpose: Autosomal dominant polycystic kidney disease is associated with an increased risk of intracranial aneurysms.
        Pubmed
        1
        The polycystic kidney disease is a hereditary malformation seldom described in Africa.
        Pubmed
        2
        Cerebral aneurysms are sometimes associated with inherited diseases like autosomal dominant polycystic kidney disease.
        Pubmed
        3
        Autosomal-dominant polycystic kidney disease is a multiorgan disease and its vascular manifestations are common and life-threatening.
        Pubmed
        4
        We report a very rare case of type I choledochal cyst associated with a polycystic kidney disease.
        Pubmed
        5
        Background and purpose: Autosomal dominant polycystic kidney disease is associated with an increased risk of intracranial aneurysms.
        Pubmed
        1
        Conclusions: The novel mutation in polycystic kidney and hepatic disease 1 gene identified by WES might be molecular pathogenic basis of this disorder.
        Pubmed
        Translations for congenital biliary ectasias