Embryology Flashcards

1
Q

What are the 4 cellular processes involved in embryological development?

A

Proliferation
Differentiation
Reorganisation
Apoptosis

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2
Q

What are the key developmental events that occur in the first 2 months of pregnancy?

A

Week 3: trilaminar disc (gastrulation), CNS, somite BVs form, placental villi (3mm)

Week 4: neural tube closes, face (limbs) initiated, placental villi elaborate (4mm)

Week 5: face + limbs continue (5-8mm)

Week 6: lots of other organs inc GIT and GU (10-14mm)

Week 7: continue and toes develop (17-22mm)

Week 8: lungs, liver and kidney (28-30mm)

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3
Q

What are the processes leading to spina bifida?

A
  • 3 weeks PF: formation of neural tube (CNS precursor)
  • Fusion should occur through neural tube
  • Does not occur
  • Location of gap in fusion process determines defect location, + tf effects
  • “2 spines” - parallel tissues either side of spine often towards lower back, usually single
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4
Q

How may a cleft palate/lip arise?

A
  • Grooves formed in midline
  • Masses of tissue migrate from lateral side of face in towards midline to fill in these grooves
  • Failure to fill these grooves leads to cleft palate/lip
  • Upper lip consists of 2 grooves –> asymmetric defect
  • Cleft palate = defect that occurs posterior to incisive foramen
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5
Q

How do the kidneys develop?

A
  • Pronephros - precursor, grows down towards cloaca
  • Gives rise to pronephric duct then begins to break down
  • Mesonephros - intermediate, connects to cloaca
  • BVs appear + mesonephros forms capsules
  • Metanephros - definitive kidney (wk 5) excretory units from metanephric mesoderm
  • Week 6-8: start down by ureters + ascend towards adrenal glands
  • Ureters extend, arteries breakdown + reform
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6
Q

What complications can occur during renal development?

A
  • Horseshoe kidney - kidneys fused below inferior mesenteric artery
  • Renal agenesis (bilateral = Potter’s syndrome due to low amniotic fluid the ureteric buds don’t grow)
  • Abnormal ureter/shaped kidneys
  • Pelvic kidney (doesn’t ascend)
  • Retention of extra artery (isn’t broken down) - may obstruct ureter –> enlarge renal pelvis
  • Bladder exstrophy - problem w/cloaca - abdominal wall fails to cover bladder - abnormal distance btwn scrotum + penis
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7
Q

How does the heart develop?

A

Week 3 - heart at midline - cardiogenic cells develop in U pattern outside embryo proper

Week 4 - heart tubes fuse

Day 23 - heart loops - atria loop posteriorly and to the right so they end up more cranial to ventricles

Day 28 - heart septation - spiralling occurs

Week 7 - outflow tracts divide

  • Vascular connections maintained, so major arteries connected to ventricles + veins to atria
  • Valves develop –> unidirectionally flow ensured
  • Foramen ovale between atria
  • Main artery from RV connected to aorta by ductus arteriosus
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8
Q

How do cardiac abnormalities can occur?

A
  • Problem w/heart looping day 23 = transposition of great arteries (aorta + PA swapped)
  • Problem with heart septation day 28 = ventricular septal defect - deoxygenated blood into LV, patent foramen ovale
  • Problem w/outflow tracts dividing wk 7 = pulmonary stenosis, truncus arteriosus
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9
Q

How is spina bifida prevented?

A

Folic acid before conception (3 months)

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10
Q

How do the lungs develop?

A
  • Begins during 1st TM, not completed until after delivery
  • Surfactant produced from 25 weeks PF + gradually increased during 3rd TM
  • 5 stages of development (wks gestational age, since LMP)
  • Week 0-6 = embryonic
  • Week 6-16 = pseudoglandular
  • Week 16-28 = canalicular
  • Week 28-36 = saccular
  • Week 36-birth = alveolar
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11
Q

How does the face develop?

A
  • 2 halves of face develop separately
  • Nasal pits begin where our eyes should be and eyes develop on sides of head
  • Between wk5 and 10 PF, nose + eyes migrate inwards
  • Eyes + nose begin on linear lvel
  • Tissue btwn nasal pits apoptose via cleft formation
  • Instead of new cell proliferation to fill up cleft, existing cells migrate centrally and pulls along with it the eyes + nose
  • Process continues until 2 halves of face fuse
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12
Q

What is the Tetralogy of Fallot?

A
  1. Pulmonary stenosis (thickened, narrow pulmonary outflow tract)
  2. Thickened RV wall
  3. Ventricular septal defect
  4. Aorta overides septal defect
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13
Q

What happens in the embryonic stage of lung development?

A

0-6 weeks gestational age:

  • Laryngotracheal groove folds into tube
  • Tube divides into oesophagus + lung buds
  • Buds grow into pleural passages + divide into lobes
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14
Q

What happens in the pseudoglandular stage of lung development?

A

6-16 weeks gestational age:

- Trachiobronchial tree forms as branching tubules resemble exocrine gland

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15
Q

What happens in the canalicular stage of lung development?

A

16-28 weeks gestational age:

  • Ascinar units form terminal bronchioles and divide into resp bronchioles
  • Capillaries approximate to potential air spaces but have little contact
  • Type 1 and 2 alveolar cells + surfactant starts being made
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16
Q

What happens in the saccular stage of lung development?

A

28-36 weeks gestational age:

  • Barrier thins
  • Increased maturation of surfactant
17
Q

What happens in the alveolar stage of lung development?

A

36 weeks gestational age-birth:

- Primitive alveoli mature

18
Q

Which cells make surfactant?

A

Type 2 alveolar cells

19
Q

What is the role of surfactant?

A

Reduces surface tension

Produces constituent apoproteins

20
Q

What causes respiratory distress syndrome?

A

Low surfactant

21
Q

How can you increase surfactant production?

A

Injecting glucocorticoids

22
Q

What layer of cells does the bladder develop from?

A

Mostly endoderm
Trigone is mesodermal (mesonephric duct)
- Trigone signals filling of bladder

23
Q

Why does the mesonephric duct break down in females?

A

Gives rise to testes

24
Q

When do the kidneys ascend?

A

Week 6-9 PF

25
Q

What happens as the kidneys ascend?

A
  • Need to rise up to lumbar region
  • Don’t drag BVs with them
  • Send out new and more cranial branches
  • Caudal branches regress
  • Mesonephros degenerates
  • Gonads descend
26
Q

Where do the gonads develop from?

A

Intermediate mesoderm within urogenital ridges

27
Q

Where do the genital ducts arise from?

A

Paired mesonephric ducts (Wolfian duct - male) + Paramesonephric duct (Mullerian - female)

28
Q

When do the genital ducts start to differentiate?

A

Week 7 PF

29
Q

What does male sex rely on?

A

Activity of SRY protein

30
Q

What are the main developmental abnormalities of the reproductive system?

A

Female:
- Congenital adrenal hyperplasia - mutation in CYP21A2

Male:

  • Androgen insensitivity syndrome - mutant androgen R
  • Result of inability to produce testosterone/anti-Mullerian hormone OR inability of target tissues to respond (Rs)
31
Q

What causes regression of the paramesonephric female ducts?

A

Testosterione
**Anti-mullerian hormone
DHT

32
Q

How do the gonads and reproductive tract develop?

A
  • Gonads arise from intermediate mesoderm within urogenital ridges of embryo
  • Genital ducts arise from paired mesonephric + paramesonephric ducts
  • Mesonephric ducts give rise to MALE genital ducts (Wolffian system)
  • Paramesonephric ducts give rise to FEMALE genital ducts (Mullerian system)
  • Gonads and RTs are indifferent up until 7 weeks of development
  • Differentiation is influenced largely by presence or absence of SRY (on Y chromosome)
  • If SRY+, then development proceeds along male path
  • If SRY-, then development proceeds along female path