Embryology Flashcards

1
Q

Mesonephric duct

A

will form the wolffian duct

forms from intermediate mesoderm
drains into cloaca

will form epididymis, ductus deferens, ejaculatory duct; seminal vesicle

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2
Q

paramesonphric duct

A

forms from intermediate mesoderm
drains into cloaca

forms the mullerian duct

will regress in males except for the appendix of the testes and prostatic utricle

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3
Q

Indifferent gonad

A

weeks 6

has outer cortex and inner medulla with primitive sex cords

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4
Q

testicular descent

A
  1. About 97% of newborns are born with descended testes; of those that remain undescended, most will descend within about 3 days after birth.
  2. Controlled by testosterone; but exact mechanism remains unknown.

pulled by the gubernaculum with the processus vaginalis

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5
Q

cloacal-urethral folds

A

mesenchymal swelling around cloacal membrane

shaft, root of penis and penile urethra

a. Elongates along with the genital tubercle.
b. Urethra groove is an open grove on ventral penis.
c. Later, the two folds fuse to form the penile urethra.
d. The remaining portion of the urethra (in the glans penis) is formed by ectodermal cells that grow inward.

later divide into urethral and anal folds

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6
Q

genital swellings

A

form on each side of cloacal membranes
(lateral)

will form the scrotum

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7
Q

genital tubercle

A

under the influence of DHT and T

will form into the glans penis and the CS and CC

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8
Q

hypospadia

A

penile urethra opens in abnormal position

  1. Caused by incomplete fusion of the urethral groove on ventral surface of penis.
    T dependent
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9
Q

epispadias

A

often with extrophy of bladder
T independent

urethral opening on top of penis

due to urethral plate developing more dorsally than normal

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10
Q

hydrocele

A

fluid filled space around the testes
tunica vaginalis are serous membranes, which become hyperactive and exs serous fluid fills the testes (usually can just be absorbed in the first few mo. of life)

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11
Q

Crytptochidism

A

testosterone dependent undescended testes

teste can be found anywhere (often in the abdomen, inguinal canal or spermatic cord)

this teste will be infertile due to temperature problems

**big risk factor for testicular cancer

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12
Q

Formation of female genitalia

A

**E2 independent

just needs the absence of MIH (AMH)

the cortex forms the ovary and the medulla regresses

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13
Q

female genital ducts

A
mesonephric ducts (wolffian) regress- MOSTLY, if they do not, they can form Gardner's cysts 
Paramesonephric ducts internal genitalia
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14
Q

cranial portion of paramesonephric ducts

A

form fallopian tubes,

unfused

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15
Q

caudal end of paramesonepthric ducts

A

fused, forms uterus, cervix and superior vagina

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16
Q

sinovaginal bulb

A

from cloaca

induced by paramesonephric ducts, inferior portion of the vagina

vagina

17
Q

genital swellings female

A

labia majora

18
Q

urethra folds

A

labia minor
erectile tissue (bulbs of vestibule and crus of clitoris)
urethral groove remains unfused and will form the vestibule

19
Q

genital tubercle

A

elongates to form the clitoris

20
Q

uterus arcuatus

A

very slight lack of fusion of PM ducts

21
Q

uterus bicornis

A

partial lack of fusion of PM ducts

2 uterine horns

22
Q

uterus didelphys

A

complete lack of fusion of PM ducts and formation of two sinovaginal bulbs

**everything is duplicated: 2 uterine horns, cervixes, vaginas

23
Q

uterus bicornis unicollis

A

only 1 uterine horn forms up with the vagina and 1 rudimentary horn

24
Q

uterus unicornis

A

on PM ducts fails to form

25
Q

Klinefelter syndrome

A

47 XXY male

nondisjunciton 
testes form (due to SRY) but are infertile due to low T levels and high E 
more female secondary sex character 
impared sexual maturation at puberty 
gynecomastia
26
Q

Turner syndrome

A
  1. 45, XO
  2. Cause: Nondisjunction during meiosis
  3. Gonadal dysgenesis(No ovaries or testes); streak gonads (Non functional genital ridge, bc you need two functional X’s)

the rest of internal and external gonads develop normal female

  1. Lack of secondary sex trait development at puberty
  2. Short-stature, broad chest, short neck; lymphedema of hands and feet
27
Q

Swyer syndrome

A
  1. 46, XY
  2. Cause: Point mutation of SRY gene resulting in defective TDF protein. (
  3. Gonadal dysgenesis; streak gonads develop. These gonads can become cancerous; often removed before puberty.
  4. Female external and internal genitalia (except for ovaries)
  5. Amenorrhea
  6. Lack of secondary sex trait development at puberty

essentially the same as Turner’s, due to the fact that you need 2 X to form ovaries)

28
Q

true Hermaphroditism

A
  1. Presence of male and female gonadal tissue (within same or opposite gonad).
  2. Ovotestes – ovarian and testis tissue found in same gonad.
  3. Most have the 46, XX genotype.
  4. Cause is most likely a translocation of portion of Y (containing SRY gene) onto X chromosome during meiosis.
  5. Ambiguous external genitalia.
29
Q

Female pseudohermaphroditism

A
  1. 46, XX
  2. Cause: congenital adrenal hyperplasia (excessive production of androgens by adrenal glands).
  3. Ovaries
  4. Internal reproductive organs usually female
  5. Masculinization of external genitalia, long clitoris, with a separate urethra
30
Q

Male pseudohermaphroditism

A
  1. 46, XY
  2. Testes form (due to normal functioning Y chromosome).
  3. Insufficient androgen production and AMH (hypogonadism)
  4. External and internal genitalia normally female

genetically male, but grow up female, need to treat with E2 at puberty

31
Q

androgen insenstivity

A
  1. 46, XY
  2. Testes (due to normal functioning Y chromosome)
  3. AMH and testosterone production is normal
  4. Lack of androgen receptors (tissues are not responsive to testosterone)
  5. Mesonephric ducts degenerate (due to insensitivity to testosterone)
  6. Paramesonephric ducts degenerate (due to presence of AMH)
  7. Female external genitalia; including secondary sex traits
  8. Vagina is short and blind-ending

**testes that do not descend, no other internal gonads