Renal embryo, A&P: random memorization Flashcards

1
Q

What is the cause of multicystic dysplastic kidney?

A

Abnormal interaction btwn ureteric bud and metanephtic mesenchyma

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2
Q

Name 3 major causes of Potter sequence

A

ARPKD
Posterior urethral calves
Bilateral renal agenesis

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3
Q

MC site of obstruction–>hydronephrosis in fetus?

A

UPJ

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4
Q

During entry to the true pelvis, how do ureters pass in relation to internal iliacs and gonadal vessels?

A

Ureters pass:
lateral to internal iliacs
medial to gonadal vessels

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5
Q

Why is the left kidney taken during living donor transplants?

A

It has a longer renal vein

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6
Q

Where does the prox 1/3 of the ureter get its blood supply?

A

Renal artery

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7
Q

Radiolabeled albumin measures what fluid compartment?

A

Plasma volume

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8
Q

Inulin measures what fluid compartment?

A

ECF

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9
Q

Does creatinine CL slightly over or underestimate GFR?

A

Overestimates

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10
Q

Does ERPF (measured by PAH CL) slightly over or underestimate RPF?

A

Underestimates (by ~10%)

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11
Q

What’s the primary size barrier of the glomerulus?

A

Fenestrations in capillary endothelium

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12
Q

What’s the primary charge barrier of the glomerulus? Be specific!

A

Heparan sulfate (negative) on fused basement membrane

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13
Q

Which portion of the nephron reabsorbs amino acids, and what type of transporter is used?

A

PT; Na-dependent

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14
Q

How do you treat Hartnup dz?

A

Niacin + high protein diet

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15
Q

How does normal pregnancy cause glucosuria and amino aciduria?

A

Causes decreased resorption of glc and aa’s in the PT

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16
Q

What’s the only autosomal dominant renal tubular defect?

A

Liddle syndrome