Urogenital Development (6) Flashcards

(33 cards)

1
Q

kidney development

A
  1. pronephroi (week 4)
  2. mesonephroi (week 4) aka embryological kidney for 4 weeks
  3. metanephroi (dev week 5, function by 9) aka adult kidneys
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2
Q

mesonephroi ducts

A

drain the mesonephroi but after degeneration (12) ducts remain and develop in males

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3
Q

metanephroi development

A

ureteric bud + metanephrogenic blastema

initial growth from bud
bud is outgrowth of mesonephric duct

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4
Q

adult derivatives

other kidney parts

A

stalk > ureter
cranial bud > collecting tubules > major and minor callices

fetal kidney has lobes dissapear in 1st year

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5
Q

renal agenesis

A

kidneys not develop so either unilateral or bilateral

if bilateral assoc w/ oligohydramnios and death

oppo of polyhydramnios, little/no amniotic fluid

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6
Q

horseshoe kidney

A

fusion at the poles so kidneys can’t rise

higher in males and females with turner’s syndrome

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7
Q

ectopic ureter

A

ureter in the ductus deferens/seminal gland/urethra/vagina = incontinence

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8
Q

urogenital sinus parts

A
  1. vesical- forms bladder and allantois
  2. pelvic- forms urethra
    -males = membranous and prostatic only
    -females = entire
  3. phallic- primordium of penis or clitoris and spongy urethra in males

glans penis from ectoderm instead of endo

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9
Q

bladder development

A
  1. bladder and allantois initially continous
  2. allantois constricts > urachus
  3. mesonephric ducts incorporated into dorsal wall of bladder
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10
Q

bladder locations

A

birth-6 yr = abdominal organ
6-puberty = greater pelvis
adult = lesser pelvis

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11
Q

urachal sinus

allantois closure problems

A

allantois doesn’t close fully so urine flow out of umbilicus

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12
Q

urachal fistula

allantois closure problems

A

allantois doesn’t close at all so free flow out of umbilicus

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13
Q

urachal cyst

allantois closure problems

A

allantois closes but urine becomes trapped in a pouch

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14
Q

gonad development

A
  1. primordial germ cells from yolk sac
  2. undifferentiated until week 6-7 with cortex and medulla
  3. cortex > ovary (medulla regress) and medulla > testis (cortex regress)
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15
Q

testes development

A
  • XY genotype
    1. SRY gene on Y starts testicular dev by **turning off **Wnt4, Foxl3, Fst, Rspo1 = inhibit ovarian dev
    2. hormones produced for functional dev
    -testosterone, DHT, AMH
    3. testes cordoned off from mesonephros by thick tunica albuginea
    4. AMH inhibits paramesonephric
    5. seminiferous tubules produce sperm @ puberty
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16
Q

ovary development

A

XX genotype
1. Wnt4, Foxl2, Fst, Rspo1 genes make functional
2. must have two X for functional dev
3. separated from mesonephros by thin tunica albuginea
4. no oogonia postnatally

no hormones needed

17
Q

genital ducts

males

A

testosterone stimulates mesonephric ducts > ductus deferens, seminal vesicles, ejac ducts

AMH degenerates paramesonephric duct

prostate and bulbourethral glands outgrowth of urethra (urogenital sinus)

18
Q

genital ducts

females

A

no testosterone = mesonephric dissapear
no AMH = paramesonephric ducts dev

estrogens from mother stim dev of uterine tubes + uterus + superior vagina from paramesonephric

greater vestibular glands and paraurethral glands form from urogenital sinus

19
Q

external genitalia

male

A

induced by testosterone

phallus enlarges/elongates = penis and encloses spongy urethra

labioscrotal swellings fuse = scrotum

20
Q

external genitalia

female

A

NOT hormonally induced

phallus shrinks = clitoris
urethral folds separate = labia minora
labioscrotal swellings stay separated = majora

21
Q

ovotesticular DSD

A

non functional sex organs
ambiguous external

have both testicular and ovarian tissue

22
Q

XX DSD

A

female fetus exposed to excessive androgens (steroids) = functional ovaries but masculine external

23
Q

XY DSD

A

inadequate testosterone and AMH by fetal testes = variable external

24
Q

androgen insensitivity syndrome

aka testicular feminization syndrome

A

XY genotype resistant to testosterone

typical female appearance but vagina ends in blind pouch

testes present and ovaries absent, no menses

testes removed for cancer prevention

25
mixed gonadal dysgenesis
XY genotype testis on one side + undifferentiated gonad on other side internal female (uterus) but external range at puberty no breasts or menses but masculinization may occur
26
5-alpha-reductase deficiency
normally converts testosterone to DHT XY genotype so typical male internal external variable but often female pre-puberty > male sex characteristics dev at puberty so indiv identifies as male | very rare
27
hypospadias | penile disorders
external urethral orifice on central surface of glans penis or body
28
epispadias | penile disorder
external orifice on dorsal surface of penis assoc w/ bladder exstrophy
29
bifid penis | penile disorders
assoc w/ bladder exstrophy and bifid anus
30
micropenis | penile disorder
fetal testicular failure and hypopituitarism (low hormones)
31
agenesis of external genitalia
failure of genital tubercule to dev so urethra opens into perineum near anus absence of vagina/uterus from failure of sinovaginal bulbs to dev
32
uterine abnormalities
1. double uterus 2. rudimentary horn 3. septum dividing uterus 4.
33
hymen abnormalities
1. incomplete perforation 2. septate hymen 3. cribiform (small dots) 4. microperforate 5. imperforate