The polycystickidney disease is a hereditary malformation seldom described in Africa.
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Cerebral aneurysms are sometimes associated with inherited diseases like autosomal dominant polycystickidney disease.
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Autosomal-dominant polycystickidney disease is a multiorgan disease and its vascular manifestations are common and life-threatening.
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We report a very rare case of type I choledochal cyst associated with a polycystickidney disease.
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Background and purpose: Autosomal dominant polycystickidney disease is associated with an increased risk of intracranial aneurysms.
1
Conclusions: The novel mutation in polycystic kidney and hepatic disease 1 gene identified by WES might be molecular pathogenic basis of this disorder.
Uso de autosomal dominant polycystic kidney disease em inglês
1
Cerebral aneurysms are sometimes associated with inherited diseases like autosomaldominantpolycystickidneydisease.
2
An intriguing feature of autosomaldominantpolycystickidneydisease (ADPKD) is the focal and sporadic nature of individual cyst formation.
3
In light of the parallels between cancer and autosomaldominantpolycystickidneydisease (ADPKD), the latter is currently being studied as a metabolic disease.
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The rate at which autosomaldominantpolycystickidneydisease (ADPKD) progresses to end-stage renal disease varies widely and is determined by genetic and non-genetic factors.
5
Background and purpose: Autosomaldominantpolycystickidneydisease is associated with an increased risk of intracranial aneurysms.
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Autosomaldominantpolycystickidneydisease is genetically heterogeneous, with at least two chromosomal loci accounting for the disease.
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Autosomaldominantpolycystickidneydisease (ADPKD) is a genetic disorder in which renal tubules become enormously enlarged due to fluid accumulation.
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Autosomaldominantpolycystickidneydisease (ADPKD) is the most common life-threatening hereditary disease and is the fourth most common cause of end-stage kidney disease.
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Autosomaldominantpolycystickidneydisease (ADPKD) is a common monogenetic disease characterized by the progressive development of renal cysts with further need for effective therapy.
Translations for autosomal dominant polycystic kidney disease