The polycystic kidney disease is a hereditary malformation seldom described in Africa.

Cerebral aneurysms are sometimes associated with inherited diseases like autosomal dominant polycystic kidney disease.

Autosomal-dominant polycystic kidney disease is a multiorgan disease and its vascular manifestations are common and life-threatening.

We report a very rare case of type I choledochal cyst associated with a polycystic kidney disease.

Background and purpose: Autosomal dominant polycystic kidney disease is associated with an increased risk of intracranial aneurysms.

My GP told me that I have polycystic kidney disease and has referred me to a nephrologist.

Conclusion: Hepatic cystic disease is common in patients that have had kidney transplants because of polycystic kidney disease.

Beneficial effects beyond changing serum tonicity and alternative uses, such as in polycystic kidney disease, need further exploration.

Autosomal dominant polycystic kidney disease is genetically heterogeneous, with at least two chromosomal loci accounting for the disease.

Conclusions: Patients with polycystic kidney disease face an increased risk during intracranial aneurysm treatment, whether by coiling or clipping.

Dialysis modality, time interval, and polycystic kidney disease were included in a linear mixed model with the outcome ERI.

EDNRA is a member of G protein coupled receptor family and is involved in cardiovascular or polycystic kidney disease.

Together, our data demonstrate multifaceted effects of sustained activation of guanylyl cyclase A on polycystic kidney and liver disease.

We sought to use ultrasonography to quantify renal size and echogenicity in a mouse model of polycystic kidney disease.

Potential therapeutic agents are now being tested in patients, moving polycystic kidney disease research into a new and exciting phase.

However, the hospital stay was not longer in the polycystic kidney group, and the total hospital charges were not higher.