Which of the following is a noninheritable form of cystic kidney disease

• Juvenille nephronophthisis

• tuberous sclerosis

• von Hippel lindau

• multicystic dysplastic kidney disease

• ARPKD

Match the following

• VHL

• Chromosome 3

• ARPKD

• Chromosome 6

• Tuberous sclerosis

• Chromosomes 9 and 16

• ADPKD

• Chromosomes 16 and 4

• Juvenile nephronophthisis/mcd

• Chromosome 2

Tags

NGSS.HS-LS3-1

Which disorder of the kidneys is autosomal dominant

• adult polycystic disease

• childhood polycystic kidney disease

• familial juvenile nephronophthisis

• multicystic renal dysplasia

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

______ is the most common hereditary cause of ESRF and is characterized by multiple expanding cysts of both kidneys that ultimately destroy the renal parenchyma and cause renal failure

• Multicystic dysplastic kidney

• Tuberous sclerosis

• ADPKD

• ARPKD

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

Chronic renal failure beginning at 40-60 years of age and berry aneurysms are characteristics of

• ADPKD

• ARPKD

• Medullary sponge kidney

• Multicystic renal dysplasia

• acquired renal cystic disease

Dull flank pain of variable severity, abdominal or flank masses, hematuria, hypertension and renal failure are associated with what renal disorder

• Polycystic Kidney Disease (PKD)
• Acute Kidney Injury
• Chronic Kidney Disease
• Nephrotic Syndrome

What dysfunctional protein is most commonly associated with autosomal dominant polycystic kidney disease (ADPKD)?

A. Fibrocystin
B. Nephrin
C. Polycystin-1
D. Polycystin-2
E. Podocin

• Fibrocystin

• Nephrin

• polycystin-1

• podocin

Tags

NGSS.HS-LS1-1

NGSS.HS-LS3-2

Dysfunction in polycystin-1 affects cilia which serve in the kidney as __________.

A. Producers of tubular fluid
B. Regulators of glomerular filtration rate
C. Mechanosensors of fluid flow
D. Transporters of electrolytes
E. Receptors for hormonal signaling

• producers of tubular fluid

• regulators of gfr

• mechanosensors of fluid flow

• transporters of electrolytes

• receptors of hormonal signaling

• ADPKD

• ARPKD

• multicystic renal dysplasia

• hereditary nephritis (alport syndrome)

• fabry disease

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2

• ADPKD

• ARPKD

• multicystic renal dysplasia

• hereditary nephritis (alport syndrome)

• fabry disease

Tags

NGSS.HS-LS3-1

NGSS.HS-LS3-2