Wu's embryo Flashcards

1
Q

Tissue origin of pouches?

A

Endoderm

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

Tissue origin of arches?

A

mesoderm

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

Tissue origin of clefts/grooves/folds?

A

ectoderm

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

**Bone and cartilage are derived from

A

Neural crest!

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

Tympanic membrane is the first membrane

A

Connects the inner ear (a pouch) to the outer ear ( a fold)

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

Each arch has an associated nerve and arterial arch

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

What arch is innervated by the superior laryngeal branch of vagus nerve?

A

Pharyngeal arch 4; derivatives:

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

Cricothyroid and posterior crycoartenoid

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

What arch is innervated by the recurrent laryngeal branch of the vagus nerve?

A

Pharyngeal arch 6; derivatives:

Remember that the ductus arteriosis becomes the ligamentum arteriosum in teh adult

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

What does cleft 1 become?

A

External auditory ematus

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

What do clefts 2-4 become?

A

Nothing- they usually get obliterated. If they aren’t obliterated, you get cystic anomalies/remnants of the neck

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

Cystic anomalies of the neck arise from failure of clefts 2-4 to be obliterated; instead they are combined into a cervical sinus on the neck. What are the 3 types?

A
  • Cervical branchial cyst
  • Thyroglossal duct/sinus
  • Ectopic thyroid gland/ nodule
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Lateral mass in front of the SCM that enlarges with age- what is it?

A

Cervical branchial cyst: grooves connect together to form a gap in your neck; if connected to the outside, it’s a fistula.

Shown as lateral mass enlarges with age

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

Midline mass on your neck tha tmoves with swallowing- what is it?

A

Thyroglossal duct/sinus: tract between tongue and thyroid is not obliterated

  • the typical remnant is the foramen cecum on the tongue
  • usually asymptomatic, but may protrude tongue

Shown as a midline mass that moves withs wallowing

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

Symptoms of hyperthyroidism and an off-midline mass represent what cystic anomaly of the neck?

A

Ectopic thyroid gland/nodule: extra thyroid tissue on gland/nodule or along the paht of hte thyroid gland

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Inner ear bones are associated with what nerve in what arch? What bone is the exception?

A

Mandibular n (V3) in the first arch.

EXCEPTION: Stapes is from arch 2, which is associated with the facial nerve (remember n to stapedius?)

17
Q

Hyoid bone is associated with what arches?

A

2 and 3

18
Q

Larynx is associated with what arches?

A

Arches 4 &6

19
Q

Treacher Collins Syndrome and Pierre Robin sequence are both problems with which pharyngeal arch?

A

The first arch. Both are bone problems, so the cause is a problem with NEURAL CREST!

20
Q

Treacher Collins Syndrome- what are the other symptoms What does it look like?

A
  • Malar hypoplasia: Failure of the upper neural crest cells in the first pharyngeal arch to develop the zygomatic arch
  • Down-slanting palpebral fissures: lateral eye slanted downwards because gravity
  • Autosomal dominant
  • Because it’s a first pharyngeal arch syndrome,
    • Conductive hearing loss (malleus/incus)
    • Small mandible
    • Malformed/absent ears (auricular cartilage)
21
Q

Pierre-Robin Sequence

A

Failure of the lower neural crest structures to form the mandible.

  • U-shaped (bilateral cleft palate): tongue pushed back; doesn’t allow palate to close
  • Upper airway obstruction
  • Autosomal recessive
22
Q

Pouch things are about organs because endoderm!

A

Arch 1 = middle ear

23
Q

DiGeorge Syndrome is caused by ___ and results in

A

Cause: Deletion of one of the arms of chromosome 22 (thus, 22q11) -> neural crest issue -> endoderm of pouch can’t communicate with bad arch

Result: hypoplasia of 3rd and 4th pharyngeal pouch derivatives

24
Q

Normal functiosn of the 3rd and 4th pouch affected in DIgeorge syndrome

A

3rd pouch

  • Dorsal wing -> inferior paraythyroid*
  • Ventral wing -> thymus

4th pouch

  • Dorsal wing -> superior parathyroid
  • Ventral wing -> lil bit of thymus
25
Q

Symptoms of digeorge syndrome

A

No parathyroid -> low serum calcium

No thymus -> no T cells -> immunocompromised

Heart septa (neural crest) defective -> tetralogy of fallot

26
Q

Parathyroid hormone - what does it do and what pourches are responsible for it?

A

Parathyroid hormone raises calcium and depends on the 3rd and 4th pouch.

27
Q

What does calcitonin do and what pouch does it depend on?

A

Calcitonin tones down calcium and comes from the 5th pouch, which gives the ultimobranchial body -> parafollicular cells in thyroid that make calcitonin

28
Q

**The face is made of 5 pieces of neural crest

A
  • 1st arch
    • 2 mandibular prominences
    • 2 maxillary prominences
  • Cranial neural crest -> 1 frontal prominence
29
Q

Cleft lip

A

Failure of fusion of maxillary and medial nasal prominence

Most common: unilateral

30
Q

Cleft palate

A

Failure of fusionof maxillary processes

31
Q

Nasolacrimal groove (often an extension of cleft lip)

A

Failure of fill in the space between maxillary + medial/lateral nasal prominence