Embryology Flashcards

1
Q

mesonephros

A

second set of kidneys that form at end of week 4 from the intermediate mesoderm
- will become functional nephrons that work until month 3
- in lower thoracic, upper lumbar
drain into mesonephric duct—>cloaca

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2
Q

Metanephros

A

functional at end of 3rd mo. from intermediate mesoderm
the definitive kidney
a) metanephric blastema: directly from intermediate mesoderm–>nephron
b) Ureteric bud: diverticula from the mesonephric duct

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3
Q

metanephric blastema

A

forms all parts of the nephron

from intermediate mesoderm

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4
Q

ureteric (metanephric) bud

A

forms everything from collecting tubules—>ureter

just a bud from the mesonephric bud

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5
Q

Kidney ascent

A

move from pelvis up to abdomen by week 9
receive new vessels and innervation as they go up,
lower vessels regress
rotate 90deg so that hilum faces medially

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6
Q

accessory renal artery/vein

A

when lower vessels do not regress during ascension
- generally asymptomatic
can cause compression of ureter —>hydronephrosis (backup of urine)

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7
Q

renal hypoplasia

A

from inadequate branching of ureteric bud and lack of differentiation of nephrons

very small kidney with few (functional) nephrons

  • asymptomatic if unilateral
  • can be persistent fetal lobulation
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8
Q

Cystic diseases

A

functional kidney replaced by large cysts
present at birth—>decreased renal function
multicystic dysplastic kidney and polycystic kidney
Autosomal recessive=cysts from collecting ducts (+renal insufficiency)

Autosomal dominant: cysts from collecting ducts and nephron

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9
Q

real agenesis

A

complete lack of renal formation
ureteric bud fails to form, or it does not have signaling to induce formation of metanephric blastema
regression of bud etc
**adrenal gland is fine

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10
Q

Potter’s sequence

A

bilateral renal agenesis
non-compatible with life due to fetus not producing urine
(can also be caused by amniotic membrane)
**due to oligohydramnios: hypoplastic lungs, Potter’s face, club foot

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11
Q

ectopic kidney

A

that does not ascend

pelvic kidney most common

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12
Q

horseshoe kidney

A

inferior parts of L and R fuse in the pelvis
ascent is blocked by inferior mesenteric a
usually asymptomatic .

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13
Q

Wilm’s tumor

A

very malignant tumor that originates in the kidney and moves towards the lungs
presents in childhood
- from WT1 gene mutation
—>un-differentiated and rapidly dividing intermediate mesoderm

associated with Denys-Drash syndrome
gonadal dysgenesis

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14
Q

WAGR syndrome

A

WT1 and PAX6 gene mutation

- wilms+ gonadal dysgeneis+ eye problems+mental retardation

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15
Q

Duplication of ureter

A

splitting of the ureter
caused by splitting of ureteric bud
can sometimes lead to duplication of kidney as well

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16
Q

ectopic ureter

A

from 2 ureteric buds
forms 2 separate ureters
the lower of the two is the normal one, the upper one is often abnormal (dilated, drains to abnormal site-i.e. urethra, vagina, vestibule)

17
Q

urachal fistula

A

allantosis/ urachus remain patent

bladder—>umbilicus (ssx: urine from umbilicus)

18
Q

exstrophy of bladder

A

ventral wall defect
when the ventral pelvic wall does not fuse completely
bladder forms externally
extrophy of cloaca is more severe (associated w/ exposure of inner bladder and rectum with imperforate anus and epispadias)

19
Q

Urorectal septum

A

layer of tissue that divides cloaca and anterior urgenital sinus and the rectum/anal canal

20
Q

Urogenital sinus: cranial (vesical) potion

A

forms bladder (not trigone-from mesonephric duct)

continuous with allantois (which becomes urachus, which will become the median umbilical ligament)

21
Q

Urogenital sinus middle (pelvic) portion

A

forms urethra in females

forms prostatic and membranous urethra in males

22
Q

caudal (phallic) portion of the urogenital sinus

A

forms penile urethra