Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

Boards High Yield > Embryology > Flashcards

Embryology Flashcards

1
Q

what process characterizes the transition from morula to blasocyst

A

water movement into the marula (ie cavitation) transforms the embryo into a blastocyte

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

steps in fertilization

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what blocks polyspermy

A

cortical granules released from the egg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

blastomere vs blastocysts

A

blastomere is just another word for the cells of the developing embryo –> it takes a different name because the cells are totipotent (each one can form a complete embryo by itself)

Blastocyst –> what used to be the morula is now fluid filled and considered to be distinguished by having 2 zones: trophoblast (future placenta) and embyroblast

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

T/F: all germ layers derive from the epiblast

A

TRUE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

when is the developing embryo most sensitive to teratogens

A

weeks 3-8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is this birth defect

A

sacrococcygeal teratoma

it is comon and consists of all tisue types because it developed from pluripotent stem cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is this birth defect

A

Sirenomelia (mn: siren songs of mermaids)

aka caudal dysgenesis

caused by insuffficient mesoderm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is situs inversus?

A

a birth defects caused by dysfunction of the cilia around primitive node and there is a complete transposition of L/R axis…

serotonin (5HT) significant in determining the assymetry of organs following tthis and can cause comlete switch of viscera (including heart) in the thorax and abdomen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the likely diagnosis?

A

fetal alcohol syndrome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
A

B - anencephaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
A

answer: B –> trophoblast

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is the role of AER (apical epidermal ridges) in development of limbs?

A

forms a thickening at the distal end of lumb buds. Produces fibroblast growth factor (FGF) which interacts with underlying mesoderm to promote limb outgrowth.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are the possible complications of osteopetrosis

A

anemia, hepatosplenomegaly, immunodificencies, cranial neuropathies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the known teratogens to cause limb and digit malformations

A
  1. drugs
    1. valproate
    2. phentoin
    3. warfarin
  2. toxins: cocaine, alcohol
  3. maternal conditions
    1. gestational diabetes
    2. varicella zoster
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What muscle group derives from the epimere?

A

intrinsic muscles of the back

(all others derive from the hypomere)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what is the condition?

A

chondroplasia (or pseudochondroplasia) activating mutation in FGFR3 (fibroblast growth factor) that impaired proliferation of cartilage in the growth plate leading to shorter long bones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the first step in endochondral ossification?

A

artery invades the middle of cartilage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What condition arises due to excessive growth hormone release after the growth plates have closed?

A

acromegaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

T/F: only myotomes derive from mesoderm

A

FALSe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q
A

All bones of the upper limb form from lateral plate
mesoderm that condenses along the central axis to
form the vasculature and skeletal components

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what are the only excepts to the rule that all muscles derive from mesoderm

A
23
Q
A
24
Q

Sonic Hedgehog Gene

Where is it produced?
What axis does it pattern?

Mutations lead to

A/W

A

SHH –> responsible for making a protein called Sonic Hedgehog. This protein functions as a chemical signal that is essential for embryonic development of the forebrain (aka prosencephalon) and eyes (Separates eyes into 2)

mn: S for Sonic and Separation into 2

Mutations –> holoprosencephaly

commonest etiology: trisomy 13 (aka Patau syndrome)

25
Q

Wnt 7 gene
Where is it produced?
What axis does it pattern?

A

Produced at apical ectodermal ridge (thickened ectoderm at distal end of each developing limb)
Dorsal Ventral Axis (i.e. it’s responsible for distally extending limbs in the right direction)

mn: 7 year olds “wanna be taller”

27
Q

Homeobox (Hox) Genes
What does it do?

Mutations result in

A

Involved in segmental organization of embryo in craniocaudal direction
makes proteins called DNA binding transcription regulators

Hox mutations –> appendages in wrong location

HOX-D13 mutation causes polydactyly and syndactyly

teratogen that can mess w/ HOX gene = isotretinoin (excessive vit A)

29
Q

FGF Gene
Where is it produced?
What does it do?

A/W?

A
  1. fibroblast growth factor
  2. Produced at apical ectodermal ridge
  3. Stimulates mitosis of underlying mesoderm, providing for lengthening limbs (mn: Fetus Growing Fingers)
  4. a/w achondroplasia/dwarfism
30
Q

Week 2

A

“2 weeks = 2 layers”
Bilaminar disc with epiblast and hypoblast

N.B the hypoblast will eventually disappear

31
Q

Week 3

A

3 weeks = 3 layers
bilaminar turns into Trilaminar disc (From dorsal to ventral, the three germ layers are ectoderm, mesoderm, and endoderm.) –> called gastrulation

  1. Primitive streak, notochord, mesoderm and its organization, and neural plate begins to form. somites begin to form
32
Q

Week 3 - week 8
By week 4
Danger?

A

Embryonic Period, (somites form from mesoderm)
Organogenesis occuring
Extremely susceptible to teratogens

day 22–> neural tube formed

34
Q

Day 0

A

Fertilization by sperm forms zygote initiating embryogenesis

35
Q

Week 1

A

things that form during week one:

  1. Morula forms
  2. blastocyst /implantatoin of blasocyst
  3. trophoblast–> becomes placenta and fetal membranes –> secretes HcG

N.B. A morula is distinct from a blastocyst in that a morula (3–4 days after fertilization) is a mass of 16 totipotent cells in a spherical shape whereas a blastocyst (4–5 days after fertilization) has a cavity inside the zona pellucida along with an inner cell mass

39
Q

Weeks 8-9

A

Start of fetal period
Fetal movement and fetus looks like a baby

40
Q

Week 10

A

Genitalia have male/female characteristics

41
Q

Gastrulation
What is established?
Starts with…

A

Process that forms the trilaminar disc
Establishes ectoderm, endoderm and mesoderm
Starts with epiblast invaginating to form primitive streak

42
Q

What comes from Surface Ectoderm?

A

Adenohypophysis (Ant Pituitary from Rathke’s Pouch), Lens, Epithelial lining of oral cavity, Sensory organ of ear, Anal canal below pectinate line, Parotid, Sweat, and Mammary glands

43
Q

Week 4

A
  • “Four” –> “folding” of trilaminar disc (cranial to caudal as well as lateral folding)
  • Neural tube formed by neuroectoderm and closes by week 4
  • Heart begins to beat at week 4 (mn: 4 chambers of heart)
  • upper and lower limb buds begin to form (mn: 4 weeks = 4 limbs)
44
Q

What comes from Neuroectoderm?

A

Brain (neurohypophysis, CNS neurons, oligodendrocytes, astrocytes, ependymal cells, pineal gland)
Retina, Optic Nerve, Spinal Cord

45
Q

week 6 (GI development)

mn: the number 6 looks like a gut

A

midgut contents (i.e. intestines) herniate through umbilical cord –> rotates around SMA –> hernia reduces by 12th week

  • failure to reduce –> simple omphalocele (n.b. if lateral embryonic folds fail, liver present in omphalocele –> “liver containing omphalocele”)
  • failure of rotation –> malrotation pathologies:
    • volvulus: small bowel twists around SMA –> ischemic damage
    • obstruction (cecum ends up in mid upper abdomen, stretching the peritoneum causing Ladd bands which cause obstructions)
    • left sided colon –> more of an anatomical variant than a pathology
46
Q

Week 5

A

connection between midgut and yok sac narrows –> “yolk stalk” (aka “vitalline duct” or “omphalomesenteric duct”) –> disappears by week 9

if it persists–> Meckel’s diverticulum (outpouching at ilium d/t vitalline duct remnant) ; cysts or polyps

n. b. meckel’s diverticulum = most common congenital abnormality of GI tract
(mn: number 5 is V –> Vitalline duct)

47
Q

What comes from Neural Crest Cells?

A

PNS (DRG, CN, Celiac ganglion, Schwann cells, ANS)
Melanocytes, Chromaffin Cells of adrenal medulla, Parafollicular (C) cells of thyroid, Schwann cells, Pia and Arachnoid, Bones of skull, Odontoblasts, Aorticopulmonary septum

48
Q

Craniopharyngioma
Origin
Histo

A

Benign Rathke’s pouch rumor with cholesterol crystals and calcification

49
Q

What comes from Mesoderm?

A

Muscle, Bone, Connective Tissue, Serous Lining of Body Cavities (Peritoneum), Spleen, CV Structures, Lymphatics, Blood, Wall of Gut Tube, Wall of Bladder, Urethra, Vagina, Kidneys, Adrenal Cortex, Dermis, Testes, Ovaries

50
Q

Mesodermal Defects

A

“VACTERL”
Vertebral defects
Anal atresia
Cardiac defects
Tracheo-Esophageal fistula
Renal defects
Limb defects (bone and muscle)

51
Q

What comes from Endoderm?

A

Gut tube epithelium (including anal canal above pectinate line)
Luminal epithelium derivatives (Liver, Lung, Gallbladder, Pancreas, Eustachian Tube, Thymus, Parathyroid, Thyroid follicular cells

53
Q

week 18

A

fetal bones start making blood

54
Q

Cleft lip results when

A

the maxillary prominence fails to fuse with the intermaxillary segment during the fifth-sixth week of embryonic development.

55
Q

what are the TORCH infections

A

Revision to TORCH mnemonic → TORCHSZ

T toxoplasmosis

O Other: Parvovirus B19, pertussis

R rubella

C CMV

H HSV, HIV, HBV

S Syphilis

Z Zika, Zoster

56
Q

​​​​​​​fetal varicella syndrome p/w

A

limb hypoplasia, microcephaly, chorioretinitis. mother p/w chicken pox

chorioretinitis this is often described as a focal vitreous infiltrate appearing as “headlights in the fog”

57
Q

Congenital CMV p/w

A

can cause jaundice, hepatosplenomegaly, and periventricular calcifications.

58
Q

Congenital rubella infection characteristically causes

A

cataracts, sensorineural deafness, a “blueberry muffin” rash (purpuric lesions signify dermal erythropoiesis), PDA (murmur)

mn: RUmbling murmur in Rubella; Rubella –> Rubbing –> Public display of affection at a bakery–> PDA and bluberry muffin rash. They can’t hear (deafness) their order being called over the sound of the espresso machine (machine like murmur)

59
Q

Congenital toxoplasmosis leads to

A

chorioretinitis, hydrocephalus, intracranial calcifications, microcephaly, and seizures. It is caused by an obligate intracellular protozoan, Toxoplasma gondii.

60
Q

DHT induces the differentiation of the ______, _________, and ______

testosterone induces the differentiation of the ______, _________, and ______

A

DHT induces the differentiation of the penis, scrotum, and prostate

testosterone induces the differentiation of the epididymis, ductus (vas) deferens, and seminal vesicles.

61
Q

what embryological event leads to tetralogy of fallot

A

Abnormal neural crest cell migration leads to anterior and cephalad deviation of the infundibular septum during embryologic development, resulting in a malaligned VSD and an overriding aorta

Boards High Yield (28 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions