16 - Anatomy of the Kidney Flashcards

1
Q

Mesonephric

A

Wolffian ducts (male)

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2
Q

Paramesonephric

A

Mullerian ducts (female

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3
Q

What occurs in development of female kidney

A

o Mesonephric duct degenerates apart from the lower portion that forms the ureteric bud
o Paramesonephric duct forms oviduct

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4
Q

Development of male kidney

A

o Mesonephric duct forms male reproductive tract and ureteric bud
o Paramesonephric duct degenerates

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5
Q

Types of embryonic kidney

A
o	3 embryonic kidneys – all formed from mesonephric duct
2x non functional
	Pronephric 
	Mesonephric
1x functional
	Metanephric kidney
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6
Q

What are metanephric kidneys formed from

A

 Ureteric bud from mesonephric duct

 Metanephric bud (blastemal) from mesenchyme

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7
Q

What does Ureteric bud form

A

Ureter, Renal pelvis, Major + Minor calyces, collecting tubules (1-3 million)
 Collecting System

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8
Q

What does Metanephric bud form

A

Renal glomerulus, capillaries, bowman’s capsule, proximal convoluted tubule, loop of henle, distal convoluted tubule
 Excretory system – nephron

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9
Q

Metanephros

A

sacral region (S1)

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10
Q

Final location of kidney

A

Upper lumbar T12

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11
Q

Ectopic kidney

A

Failure to ascend

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12
Q

Kidney agenesis

A

Failure of kidney to form
Unilateral or bilateral
Defects in ureteric bud formation

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13
Q

Bifid ureter

A

Ureter splits in two so you have duplicate kidneys or duplicate ureter

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14
Q

Pelvic kidney

A

Type of ectopic kidney where the kidney remains in the pelvic region (usually one of them)
Often the 2 fuse – pancake kidney

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15
Q

Horseshoe kidney

A

Type of ectopic kidney
Kidneys fuse in pelvic region
Form a single U shaped kidney
Cannot ascend due to inferior mesenteric artery

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16
Q

Polycystic kidneyy

A

Kidney’s develop fluid filled cysts
Autosomal dominant more common than autosomal recessive
Originally associated with defects in formation of tubules

17
Q

Where do cysts form in polycystic kidney

A

Collecting tubules - increased cell division in tubule epithelium - fill with fluid collected from glomerulus - break away from tubule

18
Q

Which mutations cause polycystic kidney

A

 85-90% - mutations in polycystin (PKD-1)

 10-15% - mutations in polycystin-2 (PKD-2)

19
Q

What are polycystins

A

in primary cilia (ciliopathy) – involved in cell adhesion, Ca2+ transport, cell cycle