Autosomal dominant polycystic kidney disease with cystic haemorrhage and infection

JH Chen, ST Wu, CC Wu - Acta Clinica Belgica, 2010 - Taylor & Francis
A 49-year-old man with adult polycystic kidney disease and chronic renal failure receiving
regular haemodialysis for 8 months presented with a 2 week history of abdomen pain, gross …

Autosomal dominant polycystic kidney disease: urologic complications and results of kidney transplantation: 217 patients

O Wetzel, M Hormi, L Le Normand… - Progres en Urologie …, 1993 - europepmc.org
The authors report a retrospective series of 217 cases of autosomal dominant renal
polycystic disease collected over a period of 30 years in the urology and nephrology …

Autosomal dominant polycystic kidney disease: observations from a university hospital in Saudi Arabia

FA Al-Muhanna, KK Malhotra, I Saeed… - Saudi Journal of …, 1995 - journals.lww.com
Thirty cases of autosomal dominant polycystic kidney disease (ADPKD) seen at King Fahd
Hospital of the University, Al-Khobar over a period of eight years, were analysed with …

Dominant renal polycystic disease

A Bourquia, B Ramdani, AJ Jabrane… - La Revue de …, 1989 - pubmed.ncbi.nlm.nih.gov
Autosomal dominant polycystic kidney disease is the third cause of end-stage chronic renal
failure (CRF) requiring dialysis and transplantation. Over a 5-year period we collected 21 …

[PDF][PDF] Autosomal recessive polycystic kidney disease presenting in adulthood. Molecular diagnosis of the family.

L Pérez, R Torra, C Badenas, J Ara, E Coll… - … : official publication of …, 1998 - researchgate.net
Nephrology Dialysis Transplantation Page 1 Nephrol Dial Transplant (1998) 13: 1273–1276
Nephrology Dialysis Transplantation Case Report Autosomal recessive polycystic kidney …

Autosomal dominant polycystic kidney disease complicating renal ectopia and managed with renal transplantation

A Connor, CE Weston, C Dick, JE Taylor - NDT plus, 2009 - academic.oup.com
A 65-year-old lady developed fever and right-sided abdominal pain. Her medical history
included renal transplantation for end-stage renal disease (ESRD) secondary to autosomal …

Autosomal recessive polycystic kidney disease

BS Kaplan, J Fay, V Shah, MJ Dillon… - Pediatric Nephrology, 1989 - Springer
The clinical features of 55 cases of autosomal recessive polycystic kidney disease
(ARPCKD) have been reviewed. Each had evidence of ARPCKD. The outcomes of 87 …

Renal cyst infection in autosomal dominant polycystic kidney disease

G Migali, L Annet, M Lonneux… - Nephrology Dialysis …, 2008 - academic.oup.com
A 56-year-old man with a medical history of autosomal dominant polycystic kidney disease
(ADPKD) and rightsided cadaveric kidney transplantation with homolateral nephrectomy in …

[PDF][PDF] Partial intestinal obstruction: a rare complication of autosomal dominant polycystic kidney disease: case report and review of the literature

J Gonçalves, R Filipe, C Santos, J Montalban… - J Bras Nefrol, 2012 - bbg01.com
Autosomal dominant polycystic kidney disease is a common disease with an estimated
prevalence of 1 in 400-1000 people. It is a multisystem genetic disorder characterised by …

[引用][C] Autosomal recessive polycystic kidney disease

A Sessa, M Meroni, M Righetti, G Battini… - Rare Kidney …, 2001 - karger.com
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited rare condition that
occurs in 1: 40,000 live births, but it is one of the most important hereditary nephropathies in …