Embryology development Flashcards

1
Q

What is involved in fertilisation?

A
  • Fusion of the oogonium ( 3 polar bodies and 1 ovum) and the spermatogonium (4 sperm bodies)
  • Sperm carries through pronucleus. Leaves behind organelles
  • Ovum released by the ovary. Fertilised in fallopian tube
  • ZYGOTE carried to uterine cavity by cilia
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2
Q

What happens in week 1

A

1-Zygote multiplies by mitosis to form MORULA
2-MORULA becomes BLASTULA
3- BLASTULA made up of inner cell mass, blastocystic cavity, TROPHOBLAST

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3
Q

What happens in week 2

A
1- blastula reaches endocrine cavity
2-TROPHOCYTE become CHORION
3-inner cell mass become flattened- BILATERAL DISC: EPIBLAST and HYPOBLAST.
4-Epiblast separated AMNIOTIC CAVITY
5-Hypoblast separates YOLK SAC
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4
Q

What is It and the function of the Chorion

A

Rearrangement of trophocyte
Mushy-no visible cell membrane
finger like projections

Function:

  • implantation
  • forms part of placenta
  • release of HMC hormone-used to detect pregnancy
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5
Q

Differences between fraternal and identical twins

A

fraternal-dizygote:

  • 2 sperm-2 ovum
  • usually females release 1 ovum per month-in some cases more than 1

Identical-monozygote:

  • 1 ovum-1 sperm
  • division occurs at a later date
  • can share placenta and amniotic cavity
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6
Q

Role and appearance of the placenta

A

-develops in 18-24 weeks
-smooth upper foetal surface, contains umbellical cord
-rough maternal surface
role:
-nutrition
-supply of gases + removal of waste
-immune

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7
Q

What happens in week 3 - general

A

1-Primitive streak forms from Epiblast
cells from primitive streak move in between epiblast and hypoblast
Forms axis of embryo.
2-Formation of trilaminar disc- specialised cells

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8
Q

What happens to the Ectoderm

A

1-Notochord formation
Dipping of cells from ectoderm-forms solid tube
2- Notochord releases chemicals which lead to formation of NEURAL TUBE

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9
Q

What happens when STI occurs

A

Cilia function impaired.
Zygote cannot be carried to endocrine cavity
Ectopian pregnancy

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10
Q

Where does the foetus get mitochondrial DNA from?

A

All organelles inherited from mother so all mDNA from mum- including possible diseases.

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11
Q

What happens to the mesoderm?

A

It separates into 3 layers:

  • Lateral- forms the peritoneum, pleura and body cavities
  • Intermediate- forms the urogenital system
  • Paraxial

Paraxial segments into somites- innervated by a pair of spinal nerves.
Somites then develop into:
-Dermatomes-move under the epidermis to form the dermis
-Myotomes- form muscles
-Sclerotomes: form bones and vertebrae

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12
Q

What happens in weeks 4-8?

A
  • Heart starts beating on day 24
  • Gut formation from the endometrium
  • Tube folding
  • 43 pair of somites
  • Urogenital system
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13
Q

What is teratogenesis and what does it involve?

A

Abnormalities during development which can be due to:
ENVIRONMENTAL: e.g. tobacco, drugs, infections
GENETIC: e.g. chromosome number/structure

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14
Q

When and what can increase the risk of teratogenesis?

How can it be prevented?

A
When:
week 1-2: very high risk-will usually end in death
week 3-8 : highest sensitivity to teratogens
Week 9-32: risk decreases
what?
-Dosage
-Exposure during critical periods
-genetic conditions of the embryo
Tests: 
-Prenatal:
blood
ultrasound
invasive
-Postnatal:
hearing
breathing
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15
Q

What does the gut give rise to (general)

A

Gut divides into foregut, mid gut and hindgut.

Ventral section of the foregut gives rise to the Lung buds and trachea in week 4.

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16
Q

How do the trachea, oesophagus and lung buds develop

A
  • Starts off as laryngotracheal grove or Diverticulum
  • Become surrounded in mesoderm
  • Lung buds enlarged
  • Tracheooesophageal septum separates trachea anteriorly to oesophagus
17
Q

How do the pleura develop

A
  • Splanchic mesoderm gives rise to visceral pleura
  • Somatic mesoderm gives rise to parietal pleura
  • Pleuroperitoneal canal present in space between them
  • Pleuropericardial folds separate heart from lungs
18
Q

How does the diaphragm develop

A

Shelf depends which is made up of 4 components:

  • Septum transversum- central tendon
  • Pleuroperitoneal membrane-primitive diaphragm
  • Dorsal mesentery of the oesophagus- crura + median portion
  • muscular ingrowth of lateral bodies-peripheral part
19
Q

Congenital abnormalities

A

Fistula: A passage abnormal or surgical which forms between a hollow organ and a body surface or between 2 organs e.g. tracheooesophageal
Atresia: A condition where a passage becomes shut
RDS: Inadequate production of surfactant- detergent used to decrease surface tension
Pulmonary hypoplasia: incomplete development of lungs
Incomplete closure of the diaphragm
Hernia: protrusion of an organ through a muscle which is supposed to contain it

20
Q

Morphogenesis of lung buds

A

Embryonic
Pseudoglandular ( 5-17 weeks): development of major airways, acinus, bronchial tree
Canalicular (16-26 weeks): specialisation of epithelium-cuboidal
Saccular (24-38 weeks): release of surfactant, alveolar separation
Alveolar (36-2-3years): further separation + increase in size of alveoli. 200-600 mill alveoli by 8 years.