Results 1 to 10 of about 30,094 (171)

Coronary aneurysms and dissections in a patient with autosomal dominant polycystic kidney disease: a case report [PDF]

Journal of Medical Case Reports
Background Autosomal dominant polycystic kidney disease is the most common hereditary kidney disorder, characterized by the progressive formation of renal cysts due to genetic mutations.
Maria Júlia Carnieletto Nicolodi, Gustavo Carnieletto Garcia, Md. José Knopfholz   +2 more
doaj   +2 more sources

Dual Monogenic Cystic Disease Case Report: Autosomal Dominant Polycystic Kidney Disease and Autosomal Dominant Polycystic Liver Disease [PDF]

Clinical Case Reports
Autosomal dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver disease (ADPLD) are inherited cystic conditions with overlapping features but distinct genetic causes and clinical courses.
Anna Katya Brossart, Kathryn Curry, Sumit Punj, Tarek Darwish, Hossein Tabriziani   +4 more
doaj   +2 more sources

Autosomal dominant polycystic kidney disease [PDF]

Canadian Medical Association Journal, 2017
Mutations in PKD1 or PKD2 cause autosomal dominant polycystic kidney disease, which proceeds to kidney failure in 70% of patients between the fourth and seventh decade of life.[1][1] Signs of autosomal dominant polycystic kidney disease (i.e., numerous cysts and enlargement of the kidneys) may ...
Matthew B, Lanktree, Arlene B, Chapman
  +5 more sources

Autosomal dominant polycystic kidney

Pan African Medical Journal, 2022
Polycystic kidney disease is a hereditary illness that causes cystic growth of the kidneys, resulting in increasing kidney enlargement and renal insufficiency, as well as a variety of extrarenal symptoms. The illness has autosomal dominant and recessive inheritance patterns, characterized by gradual but increasing enlargement of the kidneys, with renal
Rugaved Raghavendra Gudadhe, Gaurav Rajendra Sawarkar   +1 more
openaire   +3 more sources

Autosomal Dominant Polycystic Kidney Disease [PDF]

Advances in Chronic Kidney Disease, 2010
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic form of kidney disease and affects 1 in 500 to 1,000 individuals worldwide, regardless of ethnicity. It is characterized by progressive renal cyst formation, which distorts normal kidney architecture and ultimately causes 5% of all cases of end-stage renal disease (ESRD) in
V E, Torres, P C, Harris
openaire   +4 more sources

Surgical Management of Autosomal Dominant Polycystic Kidney Disease: Principles and Current Practice

Journal of Nepal Medical Association, 2023
Autosomal dominant polycystic kidney disease is the third most common cause of renal failure with no definitive treatment available that can directly target the development and growth of the cysts.
Badri Man Shrestha
doaj   +1 more source

Autosomal Dominant Polycystic Kidney Disease

Saudi Journal of Kidney Diseases and Transplantation, 1999
Schwenger Vedat, Zeier Martin
doaj   +2 more sources

Polycystic Liver Disease: A Case Report

The Indonesian Journal of Gastroenterology, Hepatology and Digestive Endoscopy, 2021
Polycystic liver disease is characterized by multiple cystic lesions on the liver. Liver cysts are typically incidental findings, with occasional complications including cyst hemorrhage, infection and rupture.
Randy Adiwinata, Natalin Allorerung, Jonathan Arifputra, Andrea Livina, Pearla Lasut, Bradley Jimmy Waleleng, Fandy Gosal, Luciana Rotty, Jeanne Winarta, Andrew Waleleng, Michael Tendean   +10 more
doaj   +1 more source

Autosomal dominant polycystic kidney disease [PDF]

BMJ, 1994
When the BMJ last published an editorial on adult autosomal dominant polycystic kidney disease1 there was no chromosomal assignment for the disorder. Two have since been recognised. The first, designated PKD-1,2 has been localised to a narrow region of about half a million base pairs on the short arm of chromosome 16, but the specific gene has not yet ...
A K, Saggar-Malik, S, Jeffery, M A, Patton   +2 more
openaire   +2 more sources

Molecular Mechanisms of Isolated Polycystic Liver Diseases

Frontiers in Genetics, 2022
Polycystic liver disease (PLD) is a rare autosomal dominant disorder including two genetically and clinically distinct forms: autosomal dominant polycystic kidney disease (ADPKD) and isolated polycystic liver disease (PCLD).
Ziqi Yu, Xiang Shen, Chong Hu, Jun Zeng, Aiyao Wang, Jianyong Chen   +5 more
doaj   +1 more source