Duke Embryology - Craniofacial Development

7/25/2019 Duke Embryology - Craniofacial Development

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Craniofacial Development

Suggested readings from

Langman's Medical

Embryology:

11th ed - Ch. 9 (Skeletal System): pp. 127-134 Ch. 16 (Head &

Neck): pp. 265-287

12th ed - Ch 10. (Axial Skeleton): pp. 133-141 Ch. 17 (Head & Neck):

pp. 260-282

Duke LEARNING RESOURCES

Click here to launch the Simbryo Head & Neck Development animation(and some really trippy music -you'll understand once the windowopens...)

I. Pharyngeal apparatus

pharyngeal arches are paired structures associated with the pharynx that contribute greatly to the

formation of the face, jaw, ear, and neck

the 1st pharyngeal arch appears at about the beginning of the 4th week and others are added more

caudally later such that there are ultimately 5 arches by the end of the 4th w eek the 5th arch fails to

form, so the arches are numbered 1, 2, 3, 4, and 6.

the entire apparatus consists of paired pharyngeal arches, pharyngeal pouches, pharyngeal

clefts (or grooves), and pharyngeal membranes (see diagram).

each pharyngeal arch consists of a core of somatic mesoderm and neural crest

mesenchyme

somatic mesoderm contributes to the arch artery (i.e. aortic arches 1-6) as well as

skeletal muscle tissue in each arch

neural crest mesenchyme develops into bone, cartilage, and/or connective tissue

in each arch.

each pharyngeal arch has a cranial nerve associated with it:

arch 1: CN V (trigeminal)

arch 2: CN VII (facial)

arch 3: CN IX (glossopharyngeal)

arch 4: CN X (superior laryngeal branch of the vagus)arch 6: CN X (recurrent laryngeal branch of the vagus)

the inside of the pharyngeal apparatus is lined by endoderm that forms infoldings or pouches

between the arches since there are 5 pharyngeal arches, there are 4 pharyngeal pouches,

the fates of which are discussed below.

the outside of the pharyngeal apparatus is covered by ectodermal that forms outer

pharyngeal clefts (or grooves) as with the pouches, there are initially 4 pharyngeal clefts, the

fates of which are discussed below.
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A. Fates of pharyngeal clefts

The pharyngeal clefts are ectodermal-lined recesses that appear on the OUTSIDE of the

pharnyx between the arches cleft 1 is between arch 1 and 2, cleft 2 is between arches 2 and 3,

etc.

1.pharyngeal cleft 1: develops into the external auditory meatus (the corresponding 1st pharyngeal

pouch develops into the auditory (or Eustacian) tube, and the intervening membrane develops into the

tympanic membrane).

Defects in the development of pharyngeal cleft 1 can result inpreauricular (i.e. in front of the

pinna of the ear) cysts and/or fistulas.

2.pharyngeal clefts 2, 3, and 4 are overgrown by expansion of the 2nd pharyngeal arch and usually

obliterated

Remnants of pharyngeal clefts 2-4 can appear in the form of cervical cysts or fistulas found

along the anterior border of the sternocleidomastoid muscle.


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B. Fates of pharyngeal arches

1. Pharyngeal Arch 1 (mandibular arch)

associated with the 1st aortic arch, which develops into part of the maxillary artery

innervated by CN V (trigeminal nerve)

splits into an upper maxillary prominence and a lower mandibular prominence

derivatives of the 1st arch are:

2. Pharyngeal Arch 2 (hyoid arch)

associated with the 2nd aortic arch, which develops into the stapedial artery

innervated by CN VII (facial nerve)

derivatives of the 2nd arch are:


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3. Pharyngeal Arch 3

associated with aortic arch 3, which contributes to the common carotid artery and proximal

segment of the internal carotid artery

innervated by CN IX (glossopharyngeal nerve)

derivatives of the 3rd arch are:


associated with aortic arch 4, which contributes to the proximal segment of the right subclavian

artery and the arch of the aorta

innervated by CN X (superior laryngeal branch of the vagus nerve)

derivatives of the 4th arch are:


associated with aortic arch 6, which contributes to the proximal segments of the pulmonary

arteries and ductus arteriosus (which becomes the ligamentum arteriosum in the adult)

innervated by CN X (recurrent laryngeal branch of the vagus nerve)

derivatives of the 6th arch are:


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The fates of the pharyngeal arches and their derivative structures can be summarized by the two figures

below:


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C. Fates of pharyngeal pouches

The pharyngeal pouches are endodermal-lined pockets that form on th eINSIDE of the pharynx

between the arches pouch 1 forms between arch 1 and arch 2, pouch 2 forms between arch 2

and arch 3, etc.


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1. Pharyngeal Pouch 1 develops into the auditory tube and middle ear cavity

2. Pharyngeal Pouch 2 forms numerous infoldings that become the crypts of the palatine tonsil later,

lymphocytes (from the thymus and bone marrow) infiltrate the underlying lamina propria to establish the

definitive palatine tonsil.

3. Pharyngeal Pouch 3 divides into a superior (or dorsal) and inferior (or ventral) portion:

dorsal portion of pouch 3: forms the inferior parathyroid glands the chief (or principal)

and oxyphil cells are derived from the endodermal lining of the pouch

ventral portion of pouch 3: forms the thymus the epithelial reticular cells (including thosethat comprise the thymic or Hassall's corpuscles) are derived from the endodermal lining of the

pouch. T-cell progenitors from the bone marrow infiltrate the cortex to establish the definitive

thymus.

4. Pharyngeal Pouch 4 also divides into a superior (or dorsal) and inferior (or ventral) portion:

dorsal portion of pouch 4: forms the superior parathyroid glands the chief (or principal)

and oxyphil cells are derived from the endodermal lining of the pouch

ventral portion of pouch 4: forms a diverticulum called the ultimobranchial body, which

releases signaling factors to induce the migration and differentiation of nearby neural crest

cellsinto parafollicular (C) cells of the thyroid gland.

Anomalous development of the derivatives of pouches 3 and/or 4 can result in ectopic or absent parathyroid,

thymic, or parafollicular thyroid tissue. The most common disorder in which this occurs is DiGeorge

syndrome, caused by a deletion in the long (or "q") arm of chromosome 22, leading to a hypoplasia of 3rd

and 4th pharyngeal pouch derivatives. Symptoms and signs of DiGeorge often include:

hypoplasia of the hyoid

thymic hypoplasia (immunodeficiency due to a lack of T-cells)

hypoparathyroidism (missing or hypoplastic inferior parathyroid glands)

outflow tract defects (neural crest in this area also contributes to conotruncal cushions of the outflow

tract)

Interestingly, the hypoplasia of the 3rd and 4th arches can also disrupt the 1st and 2nd arches,leading to the following additional findings:

micrognathia (reduced jaw)

cleft palate

hearing loss


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II. Development of the tongue

A. Anterior 2/3 of the tongue:

1. Formation: the anterior 2/3 of the tongue is derived from median and lateral tongue buds that arise

from the floor of the 1st pharyngeal arch and then grow rostrally. The tongue buds are then invaded by

occipital myoblasts that form the intrinsic muscles of the tongue.

2. Innervation of the anterior 2/3 of the tongue:

sensory innervationof the mucosa is via the lingual branch of the trigeminal nerve

taste innervation is via the chorda tympani branch of the facial nerve, except for the taste buds

in any circumvallate papilla that may be present in the posteriormost part of the anterior 2/3 of the

tongue these are innervated by the glossopharyngeal nerve.

motor innervation of the intrinsic skeletal muscles is via the hypoglossal nerve

B. Posterior 1/3 of the tongue:

1. Formation: swellings from the floor of the 3rd and 4th pharyngeal arches overgrow the 2nd arch and fuse

with the anterior 2/3 of the tongue. Thus, the posterior 1/3 of the tongue is derived from the 3rd and

4th arches and there is NO contribution of the 2nd pharyngeal arch in the adult tongue. Intrinsic

musculature is also derived from occipital myoblasts. The line of fusion of the ant erior 2/3 and posterior 1/3 of

the tongue is indicated by the terminal sulcus.

2. Innervation of the posterior 1/3 of the tongue:

sensory innervationof the mucosa is mostly via the glossopharyngeal nerve (and some vagus)

taste innervation is mostly via the glossopharyngeal nerve (and some vagus)motor innervation of the intrinsic skeletal muscles is via the hypoglossal nerve


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III. Development of the thyroid gland

is NOT derived from any of the pharyngeal pouches

arises from a midline thyroid diverticulum that forms from the endoderm in the floor of thepharynx just caudal to the 1st pharyngeal arch these endoderm cells differentiate into the follicular

cells of the thyroid gland.

neural crest cells of the ultimobranchial body migrate into the gland and give rise to the

parafollicular cells (aka C-cells) of the thyroid.

with differential growth of the embryo, the diverticulum elongates, but remains connected to the

forming tongue by a thyroglossal duct that later is obliterated the site of the opening of the

thyroglossal duct is the foramen cecum found in the midline at the terminal sulcus of the tongue.

Anomalies in thyroid development can result in ectopic thyroid tissue and/or cysts present along the

course of the thyroglossal duct, which is amidline structure (as opposed to cervical cysts, which are

remnants of pharyngeal clefts 2-4 and are found lateral to the sternocleidomastoid muscles).


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IV. Development of the skull

anterior portions (viscerocranium) are derived primarily from neural crest mesenchyme that develop

into bones via membranous ossification

bones in the floors of the cranial fossae, aka the "chondrocranium" (cribriform plate, sphenoid, petrous

temporal and clivus of the occipital), are derived from paraxial (somitic) mesoderm that develop

bone via endochondral ossification

flat bones of the cranial vault, aka the "neurocranium" (e.g. parietal and posterior occipital), are derived

from paraxial (somitic) mesoderm that develops into bone via membranous ossification.

the hyoid bone is derived from neural crest associated with pharyngeal arches II and III.the laryngeal cartilages are derived from neural crest associated with pharyngeal arches IV and VI.

the bones of the skull do not fuse together until after birth (to allow crowning of the head during

delivery and growth of the brain postnatally), leaving sutures and fontanelles that typically close at

various times postnatally:

the confluence of the lambdoid and sagittal sutures at the back of the skull marks the site

of the posterior fontanelle, which typically closes at around 3-6 months postnatally

the confluence of the sagittal, coronal, and frontal sutures at the top, front of the skull

marks the site of the anterior fontanelle, which typically closes by 1.5-2 years postnatally.

Because the brain continues to grow in size up until 6-7 years of age, premature fusion of the sutures or

fontanelles will result in abnormal shaping of the head as the brain will cause displacement of the bones thatremain unfused.

V. Development of the face

initially formed by 5 mesenchymal swellings (aka processes or prominences):

2 mandibular prominences (right and left, from 1st arch neural crest mesenchyme)

2maxillary prominences (right and left, from 1st arch neural crest mesenchyme)

frontonasal prominence (midline structure, from cranial neural crest mesenchyme)

two nasal pits develop in the ventrolateral aspects of the frontonasal prominences, thereby forming 2

lateral and medial nasal prominences

development of the face occurs via the growth and fusion of these prominences:

the mandibular prominences grow together to form a single mandible

The maxillary prominences (shown in orange below) grow toward the midline and fuse with

the lateral nasal prominences (blue). A deep groove called the nasolacrimal groove forms

between the maxillary and lateral nasal prominences on either side of the developing nose. Most

of the groove is obliterated with fusion of the maxillary and lateral nasal prominences, but a

small portion persists as the nasolacrimal duct and lacrimal sac.

Inward growth of the maxillary prominences also causes them to fuse with the medial nasal

prominences(yellow). Continued growth of the maxillary prominences combined with

regression of the frontonasal prominence pushes the two medial nasal prominences

together such the medial prominences eventually fuse to form the midline of the nose and

philtrum of the upper lip the superior portion of the frontonasal prominence grows and


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extends to form the forehead whereas the inferior portion does not grow very much, thus

allowing the medial nasal processes to fuse in the midline.

Below is a summary of the contributions of the prominences to the adult face:

Disruption of the development of any of the facial prominences can result in a variety of facial anomalies, such

as (from left to right in figures below):

hare lip (bilateral failure of maxillary and medial nasal prominences to fuse)

oblique facial cleft (unilateral failure of maxillary, medial, and lateral nasal prominences to fuse)

macrostoma (incomplete lateral merging of maxillary and mandibular processes)

median cleft lip (incomplete fusion of medial nasal prominences)frontonasal dysplasia (hyperplasia of inferior frontonasal prominence, thus preventing fusion of the

medial nasal prominences)


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VI. Development of the palate

A. Primary palate

forms via the fusion of the two medial nasal prominences in the midline (of course, this midline fusion

is driven via growth of the maxillary prominences which pushes the nasal prominences toward to the

middle)

consists of the premaxillary segment of the maxilla, which contains the four incisors and the incisivecanal

B. Secondary palate

forms via outgrowths of the maxillary prominences called the palatine shelves

initially, the palatine shelves project on either side of the tongue. With growth and expansion of the

mandible the tongue moves down, allowing the palatine shelves to grow toward the midline and fuse to

form the secondary palate, which consists of the palatine segment of the maxilla and palatine bone.

Disruption of growth of the tongue and/or mandible can therefore secondarily cause a cleft

secondary palate.


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Complete fusion of the primary and secondary palate is a complex process involving growth of the component

tissues, epithelial to mesenchymal transformation, cell migration, and programmed cell death at fusion sites

disruption of any part of this process can result in cleft palate. Given the involvement of the maxillary and

nasal prominences, cleft palate is often (but NOT always) accompanied by cleft lip.

Practice Questions

1. In craniofacial development, paraxial mesoderm contributes to which of the following?

A. occipital bone

B. muscles of the tongue

C. extraocular muscles

D. NONE of the above

E. ALL of the above

ANSWER

2. The craniofacial defect illustrated in the figure below was most likely caused by which of the following?


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A. premature fusion of the saggital cranial suture

B. premature fusion of the coronal cranial suture

C. overgrowth of the frontonasal process

D. incomplete fusion of the frontonasal and maxillary processes

E. incomplete migration and/or differentiation of cranial neural crest cells

ANSWER

3. The condition shown in the figure below was most likely caused by:

A. failure of the medial and lateral nasal processes to fuse with the maxillary process.

B. incomplete merging of the maxillary and mandibular processes.


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C. incomplete fusion of the medial nasal processes.

D. overgrowth of the frontonasal process.

E. incomplete growth of the mandibular process.

ANSWER

4. The thyroid gland is derived primarily from the:

A. 1st pharyngeal pouch.

B. 2nd pharngeal pouch.

C. ventral portion of the 3rd pharyngeal pouch.

D. dorsal portion of the 4th pharyngeal pouch.

E. foramen cecum at the base of the tongue.

ANSWER

5. Which of the following clinical findings is observed more frequently in association with DiGeorge syndrome

but not usually in Treacher Collins syndrome?

A. T-cell leukopenia

B. B-cell leukopenia.

C. pharyngeal and/or palatal abnormalities.

D. facial abnormalities.

E. external ear abnormalities.

ANSWER

6. Chromosomal analysis of a patient with DiGeorge syndrome would likely show which of the following?

A. trisomy 21

B. 46, XO

C. deletion of 22q

D. deletion of 11q

E. duplication of 17p

ANSWER

Questions 7-10 refer to the list below. Select the most appropriate structure in the list for each of the

following statements or descriptions (each labeled structure may be used once, more than once, in

combination with other structures, or not at all). If a statemen t or description refers to a structure NOT in

the list then the correct answer would be "NONE of the above."

A) pharyngeal arch 1

B) pharyngeal arch 2

C) pharyngeal arch 3

D) pharyngeal arch 4

E) pharyngeal arch 5

F) pharyngeal arch 6

7. gives rise to the stapes


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ANSWER

8. gives rise to the mandible

ANSWER

9. its derivatives are innervated by cranial nerve III

ANSWER

10. its derivatives are innervated by the hypoglossal nerve

ANSWER

Questions 11-14 refer to the diagram below. Select the most appropriate structure in the list for each of the

following statements or descriptions (each labeled structure may be used once, more than once, in

combination with other structures, or not at all). If a statemen t or description refers to a structure NOT in

the list then the correct answer would be "NONE of the above."

11. innervated by the facial nerve

ANSWER

12. innervated by the vagus nerve

ANSWER

13. innervated by cranial nerve VIII

ANSWER


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14. innervated by cranial nerve V

ANSWER

Questions 15-17 are based on the image below showing an 8-year old female and her 6-year old brother.

15. Based on the appearance of these two siblings, which pharyngeal arch appears to be most affected?

A. pharyngeal arch 1

B. pharyngeal arch 2

C. pharyngeal arch 3

D. pharyngeal arch 4

E. pharyngeal arch 6

ANSWER

16. Craniofacial syndromes often affect more than one pharyngeal arch. Which of the following clinical findings

would indicate the involvement of pharyngeal arch 2 in this particular case?

A. absence of the malleus (as determined by radiography)

B. hypoplasia of the hyoid (as determined by radiography)

C. hypocalcemia

D. immunodeficiency

E. hypothyroidism

ANSWER

17. Which of the following could you expect to find upon further examination?

A. palatal abnormalities

B. maxillary abnormalities

C. hearing loss

D. NONE of the above

E. ALL of the above

ANSWER

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Updated 12/6/11 - Velkey

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Duke Embryology - Craniofacial Development