GU Embryology Flashcards

1
Q

kidenys, ureters, bladder form from which layer?

A

intermediate mesoderm

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2
Q

3 stages of the kidney

Which is the adult kidney derived from?

A

1) pronephros
2) mesonephros
3) metanephros

Adult kidney is derived from metanephros

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3
Q

excretory unit forms form _____

A

mesonephric tubules

Mesonephric tubules form Bowman’s capsule, glomerulus, renal corpuscle.

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4
Q

mesonephroi (function, time functional, regression)

A

Produce small amounts of urine.
6th-12th weeks.

Regress in FEMALEs, persist in males as genital duct system

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5
Q

ureteric bud

A

Branched from caudal end of mesonephric duct.

Forms collecting system of kidney (collecting ducts, calyces, ureter)

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6
Q

two structures that form the kidney

A

ureteric bud

metanephric blastema

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7
Q

metanephric blastema

A

Forms the rest of the kidney that the ureteric bud does not form.

Ureteric bud penetrates metanephric blastema and bifurcates

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8
Q

cloacal region is divided by _________________ into a ventral _________ and a dorsal ___________

A

cloacal region is divided by urogenital septum into a ventral urogenital sinus and a dorsal anorectal canal

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9
Q

ascent of kidneys

A

Form in sacral area.
Ascend to lumbar region by differential growth of the body.

Revascularized. If original vessels do not regress, then accessory renal arteries are present.

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10
Q

horseshoe kidney

A

Inferior poles of two mesonephroi fuse during ascent of kidneys.
Cannot migrate further up than the origin of the IMA

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11
Q

pelvic kidney

A

Failure of migration of one/both kidneys.
Kidney is retained in the pelvis.
No adverse effect on kidney function

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12
Q

renal agenesis

A

Kidney fails to develop.
Due to faulty tissue-tissue interactions between ureteric bud and nephrogenic mesenchyme

bilateral can be fatal (potter syndrome)

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13
Q

potter syndrome

A

Bilateral renal agenesis.
Oligohydramnios compresses fetus.
Stillborn or die soon after birth.

(amniotic fluid is largely made from fetal urination )

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14
Q

duplication of ureter

A

Variable in length.

Occurs if initial branching of ureteric bud is not incorporated into developing kidneys.

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15
Q

urachal cyst

A

Small patent area of the urachus.

Only detected if it becomes infected.

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16
Q

urachal sinus

A

Lumen in superior portion of urachus remains patent.
Opens at urachus.
Fluid is from endothelial lining, not urine

17
Q

urachal fistula

A

Rare.
Entire urachus remains patent.
Allows urine to exit from urachal orifice.

18
Q

SRY (what it encodes, what that does)

A
SRY = Sex-determining region of the Y chromosome.
Encodes TDF (testes-determining factor).

SRY directs differentiation of Sertoli cells (directs male development).

In ABSENCE of SRY/TDF, female development occurs.

19
Q

absence of testosterone on mesonephric ducts, paramesonephric ducts

A

Mesonephric ducts degenerate.

Paramesonephric ducts give rise to female reproductive system.

20
Q

presence of testosterone on mesonephric ducts, paramesonephric ducts

A

Mesonephric ducts remain.

Paramesonephric ducts degenerate.

21
Q

paramesonephric ducts develop into (male and female)

A

FEMALE:
Uterine tubes, uterus, cervix, superior 2/3 of vagina, Hydatid of Morgagni

MALE:
appendix testes

22
Q

mesonephric ducts develop into (male/female)

A

FEMALE:
appendix vesiculosa, Gartner’s duct

MALE:
epididymus, ductus deferens, seminal vesicles, ejaculatory duct

23
Q

mesonephric tubules develop into (adult male/female)

A

FEMALE:
epoophoron, paraoophoron

MALE:
efferent ductules, paradidymus

24
Q

phallus develops into (adult male/female)

A

FEMALE:
clitoris

MALE:
glans and body of penis

25
Q

urogenital folds develop into (adult male/female)

A

FEMALE: labia minora

MALE: penile raphe

26
Q

labioscrotal folds develop into (adult male/female)

A

FEMALE: labia majora, mons pubis

MALE: scrotum, scrotal raphe

27
Q

gubernaculum develops into (adult male/female)

A

FEMALE: ovarian ligament

MALE: gubernaculum testes

28
Q

didelphic uterus

A

Paramesonephric ducts fuse to urogenital sinus separately.

2 vaginas, connected to own uterus separately

29
Q

unicornate uterus

A

One entire Mullerian duct regresses or fails to elongate.

30
Q

hypospadias

A

Urethra opens onto VENTRAL (underside) surface of penis.

Failure of urogenital folds to fuse normally

31
Q

epispadias

A

Urethra opens on DORSAL side of penis.

Failure of urogenital folds to fuse normally

32
Q

testicular hydrocele

A

Lumen between tunica vaginalis and peritoneal cavity fills with serous secretions.

33
Q

cryptorchidism

A

Undescended testes.

34
Q

male pseudohermaphroditism

A

Genetic males with feminized genitals.

Androgen insensitivity syndrome (androgens do not work on target cells).
5-alpha reductase deficiency (cannot make dihydrotestosterone).

35
Q

female psuedohermaphroditism

A

Genetic females with masulinized genitals.

Disorder of adrenal glands that cause excessive production of androgens.

36
Q

klinefelter syndrome

A

Extra X chromosome in males (XXY).
Failure of Leydig cells to produce sufficient amounts of male steroids.
Small testes, azoospermia/oliogospermia.
Gynecomastia, eunuchoidism

37
Q

turner syndrome

A

45X or 46XX/45X mosaicism.
Failure of normal sexual maturation at puberty, short stature, webbed neck, coarctation of aorta, cervical lymphatic cysts