Noun:

পলিসিস্টিক কিডনি রোগ,

polycystic kidney disease's Usage Examples:

Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease.

polycystic kidney disease.

Mutations in this gene have been associated with autosomal dominant polycystic kidney disease.

of PKD1 are associated with most cases of autosomal dominant polycystic kidney disease, a severe hereditary disorder of the kidneys characterised by.

Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent, potentially lethal, monogenic human disorder.

recessive polycystic kidney disease (ARPKD) is primarily diagnosed in infants and young children while autosomal dominant polycystic kidney disease (ADPKD).

PLD is commonly seen in association with autosomal-dominant polycystic kidney disease, with a prevalence of 1 in 400 to 1000, and accounts for 8–10%.

Studies in several animal models of polycystic kidney disease have shown a reduction in kidney size and cyst volume after treatment.

of polycystic kidney disease.

number of cell surface receptors, including adhesion-GPCRs and polycystic kidney disease proteins PKD1 and PKD2.

characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system.

Farmer died on April 1, 2020 after a long-term battle with polycystic kidney disease.

It has in vitro and in vivo activities against mouse models of polycystic kidney disease and pancreatic cancer, but its physical properties and severe.

Caroli disease is also associated with liver failure and polycystic kidney disease.

include diabetes, high blood pressure, nephrotic syndrome, and polycystic kidney disease.

PKD (Polycystic Kidney Disease) domain was first identified in the polycystic kidney disease protein, polycystin-1 (PKD1 gene), and contains an Ig-like.

Synonyms:

renal disorder; kidney disease; PKD; nephropathy; nephrosis;

Antonyms:

compound; rough; difficult; simplicity;