7.2 Development of the female genital system Flashcards

1
Q

The testes and ovaries develop from the _________________ → medial part of the urogenital ridge (in the dorsal wall of the embryo):
• Germ cells do not appear in the genital ridges until the 6th week of development
• Lateral part of the urogenital ridge is the ______________

A

genital ridge (intermediate mesoderm);

nephrogenic ridge (develops into kidneys)

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2
Q

The genital ducts arise from the paired mesonephric (Wolffian) ducts and paramesonephric (Müllerian) ducts:
• Development and regression of either duct depends on the presence of the __________________ on the Y chromosome (only found in males)

• Epithelium of the genital ridge proliferates and penetrates the underlying mesenchyme to form the primitive sex cords (indifferent gonads)
o In females (no SRY): no Sertoli cells (no ____________) → ___________ development which give rise to _____________ and no Leydig cells (no _____________) → ___________ degenerate

• Primordial germ cells (PGCs) develop in the ________________ → migrate along the dorsal mesentery of hindgut → invade genital ridges
o Inductive influence on the development of the gonad → do not develop if PGCs do not arrive at the genital ridges

A

SRY (sex determining region Y) gene

Müllerian inhibiting substance;

fallopian tubes, uterus, upper part of vagina

Testosterone;

woffian ducts

wall of the yolk sac;

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3
Q

In female embryos (XX sex chromosome complement; no Y chromosome), the primitive sex cords dissociate into irregular clusters:
• Clusters eventually degenerate and are replaced by vascular stroma (ovarian medulla)
• 7th week: surface epithelium gives rise to a second generation of cords (___________) which penetrate underlying mesenchyme but remain close to the surface. The central portion is called the medulla, which mainly contains ___________ while the peripheral part is called the cortex which contains ________________. Medullary cords disappear and cortical cords develops in the ovary.
• 4th month: cords split into isolated cell clusters → each surrounding ≥ 1 PGCs (eventually develop into ________and the surrounding epithelia cells form form ________________)

A

cortical cords;

the blood vessels;

ovarian follicles;

oogonia ;

follicular cells

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4
Q

The gonads develop in the _______________ and descend to their adult anatomical positions (_______ for testes; ________ for ovaries) before birth:

• Female gubernaculum attaches the caudal end of the ovary to the labia majora → leaves behind 2 ligaments by birth

  • Ligamentum ovary: Part between the ______________
  • Round ligament of uterus: Part between the uterus and labia majora (passes through the _______________ → ___________ → _______________)
A

abdomen;

scrotum;

pelvis;

ovary and uterus ;

deep inguinal ring;

inguinal canal;

superficial inguinal ring

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5
Q

Initially, both male and female embryos have two pairs of genital ducts: mesonephric ducts and paramesonephric ducts.
- In the absence of SRY, the gonad develops into an __________.
Sinceno testosteroneis produced, themost of the _______________ regress in female embryos.
- Since there is alsono Mullarian inhibiting substance (produced by ________),the________________ persistin female embryos

A

ovary;

mesonephric ducts;

Sertoli cells;

paramesonephric ducts

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6
Q

The paramesonephric (Müllerian) ducts eventually give rise to the uterine (Fallopian) tubes, uterus and upper third of the vagina:

  • Cranial vertical and horizontal parts of paramesonephric ducts develop into the ____________
  • Caudal parts fuse to form the __________ that projects into the dorsal wall of the urogenital sinus.
  • Uterine canal gives rise to _________________
A

uterine tube;

uterine canal;

uterus and upper 1/3 of vagina.

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7
Q

Mayer Rokitansky Küster Hauser (MRKH) syndrome: agenesis of the Müllerian system leads to complete absence of the __________________
- 2nd most common cause of primary amenorrhoea (still very rare)

A

reproductive tract (including upper vagina, uterus, Fallopian tubes)

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8
Q

what causes a unicornuate uterus?

A

Developmental arrest of 1 Müllerian duct

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9
Q

what causes a didelphic uterus?

A

Complete non-fusion of Müllerian ducts (may have 2 vaginas and simultaneous pregnancies)

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10
Q

what causes a bicornuate uterus?

A

Partial/ complete fusion of Müllerian ducts

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11
Q

what causes a septate uterus?

A

Fusion but failure of midline remodelling or resorption of tissue (septum)

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12
Q

what causes arcuate uterus?

A

Least severe; small indent in midline

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13
Q

Vagina has dual origin

  1. Upper 1/3 of the vagina develops from the ________________
  2. Lower 2/3 of the vagina develops from the _________________
A

uterine canal (paramesonephric ducts);

urogenital sinus (ventral division of the cloaca)

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14
Q

Transverse vaginal septum: generally found between the _____________ of the vagina
• Due to failure of degeneration of the ______________
• May be surgically corrected
• Associated with a shortened vagina

A

upper 1/3 and lower 2/3;

vaginal plate

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15
Q

Imperforate hymen: failure of perforation after birth
• Complete obstruction of the vagina
• Commonly diagnosed in adolescence when __________ accumulates in the vagina
• May be surgically incised

A

menstrual blood

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16
Q

Development of the External Genitalia – Indifferent Stage

  • Mesenchymal cells proliferates around the cloacal membrane to form a pair of slightly elevated ___________.
  • Cranial to the cloacal membrane the folds unite to form the _____________.
  • Caudally the folds are subdivided into urethral folds anteriorly and _____________ posteriorly.
  • Another pair of elevations, the genital swellings, becomes visible on each side of the urethral folds.
  • At the end of the sixth week, however, it is impossible to distinguish between the two sexes.
A

cloacal folds;

genital tubercle;

anal folds;

17
Q

Development of female external genitilia
- Genital tubercle forms the ___________
- Urethral folds do not fuse develop into the ____________.
Genital swellings enlarge and form the _______________.
- The urogenital groove is open and forms the vestibule

A

clitoris ;

labia minora;

labia majora

18
Q
Androgen insensitivity (testicular feminisation) syndrome (46XY): Occurs in genetic males → androgen receptor mutation (insensitive to testosterone):
• Presence of SRY: \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ regress
• No response to testosterone: \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ degenerate → external appearance of normal females (with poorly developed male internal genitalia)
A

Müllerian ducts;

Wolffian ducts

19
Q

________________: SRY gene mutation → gonadal dysgenesis → phenotypically female (normal external female genitalia, uterus, Fallopian tubes)

A

Swyer syndrome (46XY)

20
Q

Female pseudo-intersexuality (pseudohermaphroditism) (46XX): Genetic female (ovarian tissue histologically):
• Masculinisation of female external genitalia (enlarged clitoris, partial fusion of labia majora)
• Most commonly caused by ______________ (foetus produces excess androgens)

A

congenital adrenal hyperplasia

21
Q

Male pseudo-intersexuality (46XY): Genetic male (testicular tissue histologically):
• Underdeveloped male external genitalia
• Most commonly caused by _____________________

A

inadequate production of testosterone and MIS by foetal testes