Polycystic kidney disease

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder and the fourth cause of death of end-stage renal disease. The disease has a prevalence of 1:400–1:1000 accounting for 10% of patients on dialysis. In most ADPKD patients, bilateral kidneys are similarly affected, with numerous fluid-filled cysts arising from different nephron segments.

4p vitiki 30-01-2024 7 2   Download

Ebook "Cell division machinery and disease" critically evaluates the causal link between cell division machinery and disease. Further, it identifies key open questions in the field and the means for exploring them. Throughout the various chapters, internationally known contributors present the evidence for and against a causal link between key elements of the cell division machinery and diseases such as cancer, neuropathologies, aging, and infertility.

241p lucchinguyen 28-12-2023 4 2   Download

The application of WES in identifying mutations in ADPKD has been widely performed by researchers worldwide; however, in Vietnam, the utilization of WES in ADPKD studies is still limited. In this study, we applied WES to identify pathogenic variants for Vietnamese ADPKD patients and validated the obtained variants in the family using Sanger sequencing.

7p vihawkeye 26-05-2023 6 2   Download

Autosomal dominant polycystic kidney disease is one of the most common genetic renal diseases. Cyclooxygenase plays an important role in epithelial cell proliferation and may contribute to the mechanisms underlying cyst formation. The aim of the present study was to evaluate the role of cyclooxygenase inhibition in the cyst progression in polycystic kidney disease.

9p vinasaki2711 12-11-2019 12 1   Download

part 2 book “practical nephrology” has contents: renal stone disease, kidney cancer, inherited renal tumour syndromes, polycystic kidney disease, other cystic kidney diseases, inherited metabolic disease, anaemia management in chronic kidney disease, setting up and running a haemodialysis service, peritoneal dialysis prescription,… and other contents.

467p tieu_vu13 06-08-2018 34 1   Download

(BQ) Continued part 1, part 2 of the document Pediatric radiology casebase presents the following contents: Torsion of theappendix testis, collecting system duplication ectopic ureter ureterocele, posterior urethral valves, autosomal recessive polycystic kidney disease, acute pyelonephritis, angerhans cell histiocytosis, developmental dysplasia of the hip, respiratory distress syndrome,...

220p thangnamvoiva3 01-07-2016 43 2   Download

Tham khảo sách 'novel insights on chronic kidney disease, acute kidney injury and polycystic kidney disease edited by soundarapandian vijayakumar', y tế - sức khoẻ, y học thường thức phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả

144p xumxaxumxit 15-04-2013 58 4   Download

TRPP2, also called polycystin-2, the gene product ofPKD2, is a membrane protein defective in 10–15% of cases of autosomal dominant polycystic kidney disease. Mutations in PKD2 are also associated with extrarenal dis-orders, such as hepatic cystogenesis and cardiovascular abnormalities.

9p inspiron33 23-03-2013 33 2   Download

Children who have congenital heart defects or who have rheumatic heart disease may develop infective endocarditis in which the endocardial tissue is infected by organisms such as Streptococcus viridans, Staphylococcus aureus, or Staphylococcus epidermidus. The child presents with general malaise, arthralgia, fever, splenomegaly and the signs of their underlying heart disease. The classical signs of splinter haemorrhages, petechiae, haemorrhagic lesions (Janeway lesions), tender Osler’s nodes, or Roth’s spots (retinal haemorrhage) are not always seen in children.

10p connhobinh 10-12-2012 58 2   Download

Tham khảo sách 'novel insights on chronic kidney disease, acute kidney injury and polycystic kidney disease', y tế - sức khoẻ, y học thường thức phục vụ nhu cầu học tập, nghiên cứu và làm việc hiệu quả

144p wqwqwqwqwq 21-07-2012 76 10   Download

I have been involved in the treatment of chronic renal insuffi ciency for 40 years, beginning with peritoneal dialysis immediately after graduation from medical school in 1965, then with hemodialysis in 1967 after I fi rst experienced it in Kanazawa, and with renal transplantation since 1972, when I was studying in the United States. During this period, the number of dialysis patients has continued to increase rapidly to the present fi gure of 257 765 (at the end of 2005), and with surprising increases in the survival rate.

118p 951864273 09-05-2012 72 14   Download

Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài:Autosomal dominant polycystic kidney disease with diffuse proliferative glomerulonephritis - an unusual association: a case report and review of the literature

5p thulanh28 15-12-2011 33 2   Download