Early Embryology Flashcards

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1
Q

decreased AFP seen with what syndrome

A

downs syndrome

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2
Q

three periods based on fertilization age

A

0-3 weeks: early embryo

3-8 weeks: embryonic organogenesis

8-38 weeks: fetal period

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3
Q

major events week 1

A

cleavage

morula enters uterus

zona pellucida breaks down

blastulation

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4
Q

two layers of blastocyst

A

embryoblast and trophoblast

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5
Q

implantation occurs when

A

5-6 days after fertilization

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6
Q

decidua

A

endometrium of pregnancy

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7
Q

trophoblasts turns into what two layers

A

cytotrophoblast (mitotically active inner layer)

and syncytiotrophoblast (adjacent to maternal blood supply, produces hCG)

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8
Q

hydatidiform moles

A

2 types

  1. complete: fertilization of empty oocyte, fetus is entirely missing
  2. partial: oocyte with two sperm (or diploid sperm)

causes high hCG, severe nausea and vomiting, vaginal bleeding, spontaneous abortion

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9
Q

major events week 2

A

embryoblast changes into epiblast and hypoblast

2 cavities form: amniotic cavity and primitive yolk sac

extraembryonic mesoderm forms between yolk sac and cytotrophoblast (which then makes chorionic cavity)

(trophoblast has greater growth than embryoblast)

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10
Q

two sections that embryoblast transofrms into

A

epiblast (inner, columnar cells related to amniotic cavity)

hypoblast (outer cuboidal cells adjacent to yolk sac)

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11
Q

two layers of extraembryonic mesoderm

A

somatic: lines trophoblast and amnion
splanchnic: lines yolk sac

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12
Q

3 layers of chorion

A
  1. extraembryonic somatic mesoderm
  2. cytotrophoblast layer
  3. syncytiotrophoblast layer
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13
Q

oligohydramnios

A

low volume (<500mL) of amniotic fluid

  • Causes
    • low placental blood flow
    • renal agenesis or obstructive uropathy
  • complications (Potter Sequence)
    • pulmonary hypoplasia
    • facial defects and limb defects
    • compression of umbilical cord
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14
Q

polyhydramnios

A

high (>2L) amniotic fluid

  • Causes:
    • fetus does not swallow usual amount of fluid (CNS anomalies)
    • esophageal atresia
  • complications:
    • premature rupture of membranes/premature birth
    • intrauterine growth restriction
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15
Q

major events week 3

A
  • gastrulation
    • epiblast cells become motile and converge on the midline of dorsal disc forming primitive streak
    • primitive groove makes opening for cells to migrate ventrally
    • thickening at end forms primitive node and pit
  • epiblast layer gives rise to 3 germ layers
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16
Q

3 germ layers of epiblast

A
  • Endoderm: epiblast cells that replace entire hypoblast layer
  • Mesoderm: from cells that migrate between existing layers
  • Ectoderm: cells that remain in epiblast after gastrulation completes
17
Q

sacrococcygeal teratoma

A

forms from primitive streak persists longer than it should, causing cell proliferation and tumor formation in sacral area

18
Q

notochord develops from

A

migrating mesoderm cells

19
Q

direction of neural tube closure

A

cranial to caudal (and cranial end closes ~2 days before caudal end, during week 4)

20
Q

derivatives of surface ectoderm

A
  • epidermis, nails, hair, subcutaneous glands, mammary glands, anterior pituitary, enamel, lens of eye
21
Q

derivatives of neural ectoderm

A

CNS, retina, posterior pituitary gland, pineal body

22
Q

paraxial mesoderm

A
  • organizes into somitomeres in head region (then into somites, number correlates with age)
    • each somite has its own sclerotome, myotome, dermatome
    • gives rise to majority of axial skeleton (vertebal column, base of skull, ribs)
23
Q

intermediate mesoderm

A

gives rise to urogenital system

24
Q

lateral plate mesoderm

A

makes body (somatic mesoderm and overlying ectoderm) wall and gut wall (splanchnic mesoderm and underlying endoderm)

forms bones of limbs, sternum, pelvic girdle and shoulder girdle (appendicular skeleton)

25
Q

what makes gut (fore/mid/hind)

A

endoderm (and yolk sac in hindgut)

26
Q

meckels diverticulum

A

aka ileal diverticulum

  • most common congenital defect of GI system
  • due to persistence of vitelline duct
  • no symptoms (but can contain ectopic gastric or panceatic mucosa)
27
Q

embryological sources of bone are

A

paraxial mesoderm

lateral plate somatic mesoderm

neural crest cells (ectomesenchyme)

28
Q

which skull bones by neural crest cells

A

frontal, sphenoid, squamous temporal, nasal, lacrimal, zygomatic, maxilla, incicive, mandible

29
Q

which bones arise via intramembranous ossification and when

A

majority of bones of face and flat bones of skull, clavicle

end of week 7 of development

30
Q

what bones arise via endochondral ossification

A

long bones of extremities, pelvic and shoulder girdle, vertebral column

31
Q

time frame of endochondral bone formation

A
  • 6 weeks: hyaline cartilage bone model forms
  • 8-12 weeks: primary centers of ossifaction are formed
  • 38 weeks: some secondary centers of ossification are present
  • after birth: most secondary centers of ossification are formed