Development 2 Flashcards

1
Q

Whar are the 2 parts of the pituitary developed from

A

• The pituitary has ectoderm AND neurectoderm origins

• Rathke’s pouch is the Ectoderm component
- Anterior pituitary

• Infundibulum is Neurectoderm component (derived from neuroectoderm)
- Posterior pituitary and stalk

Little bit of ectoderm becomes specialised - grows up as rates pouch. Infundibulum grows down - a bit of neuroectoderm. They join together
Then bones get ossified. Removes link between rathkes pouch and oropharynx.

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2
Q

Descirb the infunibulum

A
  • Neural tube component
  • Downward out-growth of the forebrain
  • grows towards the roof of the pharynx
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3
Q

What is rathkes pouch

A
  • Out-pocketing of ectoderm of the stomatodeum
  • An evagination of the roof of the (oro-) pharynx
  • Grows dorsally towards the developing forebrain
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4
Q

What is the lingual frenulum

A

Cord that tethered the base of tongue to floor of oral cavity

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5
Q

What is the sulcus terminalis

A

Boundary between anterior 2/3 and posterior 1/3 of the tongue
V shape
Point of the V is the foramen cecum

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6
Q

When does the tongue begin to develop

A

• Primordia of the tongue appear at about the same time as the palate begins to form
• Receives a component from
each of the Pharyngeal arches

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7
Q

What are the lingual swellings

A

Lingual swellings grow up from loot of pharynx. Each is a mass of tissue.

• 2 lateral lingual swellings
From Ph Arch 1

• 3 median lingual swellings:

  • Ph Arch 1: Tuberculum impar
  • Ph Arch 2 & 3 (+4): Cupola
  • Ph Arch 4: Epiglottal swelling
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8
Q

How do the lingual swellings develop

A

• Lateral lingual swellings over-grow the tuberculum impar
• The 3rd arch component of the
cupola over-grows the 2nd arch component
• Extensive degeneration occurs,
freeing tongue from the floor of the oral cavity
• lingual frenulum - mainatains connection

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9
Q

Describe teh sensory innervation of the tongue

A
  • Mucosa of anterior 2/3s derived from Ph As 1 & 3 therefore General sensory innervation CN V & IX
  • Posterior 1/3 derived from Ph A 3 (& 4) therefore General & special sensory CN IX & X

• taste buds develop in papillae - Special sensory innervation CN VII

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10
Q

Describe the development of chorda tympani

A
  • branch of CN VII, nerve of second arch • BUT
  • passes into first arch
  • THEREFORE
  • passes through middle ear (which is a structure which develops between ph arch 1-2)
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11
Q

Describe teh motor innervation of the tongue

A

• Both intrinsic & extrinsic muscles of the tongue develop from myogenic precursors that MIGRATE into the developing tongue
• CN XII
Myogenic precursors come from somites.. each somite receives a branch from the cn xii. Move caudal to cranial, taking cn xii with them. Allows function of the tongue movement - changing shape and position

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12
Q

Where foes the thyroid gland initially appear

A

• Primordium of the thyroid gland appears in
the floor of the pharynx between the tuberculum impar and the cupola
• Final position is anterior neck
• HOW????

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13
Q

Describe the descent of the thyroid

A
  • Point of origin for the descent of the thyroid is later marked by foramen cecum
  • Bifurcates and descends as a bi-lobed diverticulum connected by the isthmus
  • During its descent the thyroid gland remains connected to the tongue by the thyroglossal duct
  • Pyramidal lobe (remnant of duct)
  • Approx 50% of population
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14
Q

What a re some thyroid abnormalities

A

• Thyroglossal cysts & fistulae
Fluid filled cyst -
Sometimes duct can have abnormal opening onto surface - fistulae but these are less common
• Ectopic thyroid tissue - At some point along the descent - some gets left behind

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15
Q

How can you tell the difference between a thyroglossal cyst and a bronchial cyst

A

Thyroiglossal cyst will like along path of decent of thyroid. A bronchial cyst is a remnant of one of the pharyngeal cleft - the anatomical landmark to determine is the SCM

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16
Q

What is fist arch syndrome

A

• First arch syndrome
• spectrum of defects in development of the eyes, ears, mandible &
palate
• Thought to result from failure of colonisation of the 1st arch with
neural crest cells
• Example – Treacher Collins Syndrome

17
Q

What is treacher-Collins syndrome

A

• Characterised by hypoplasia of mandible & facial bones
• Inherited, autosomal dominant condition
• Haploinsufficiency of Treacle, a serine/alanine rich nucleolar phosphoprotein. It is involved in
ribosomal DNA gene transcription as well as in processing of the pre-ribosomal RNA. Deficiency of
treacle leads to insufficient ribosome biogenesis, and impacts on NC migration

18
Q

Describ eteh syndromes resulting from the abnormal deveopment of first and second pharyngeal arches

A

Ss

19
Q

What is di-George syndrome

A
  • Congenital thymic aplasia & absence of parathyroid glands
  • Syndrome including a variety of additional defects
  • “C!TCH22”
  • Deletion on Chromosome 22
  • Disruption of development of 3rd and 4th pharyngeal pouches
  • Abnormal development of neural crest
20
Q

What is charge syndrome

A
• CHD7 (chromodomain helicase DNA- binding domain, ATP-dependant
chromatin remodeller) 
• CHARGE syndrome
  - CHD7 heterozygous mutation
• CHD7 expression essential for the
production of multipotent NC