Development of Skull (Embryology) Flashcards

1
Q

bones of face and skull come from

A

neuroectoderm –> neural crest in head –> mesenchyme in pharyngeal arches

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2
Q

base of skull comes from

A

intraembryonic mesoderm –> paraxial mesoderm –> somitomeres/somites –> sclerotome

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3
Q

= brain case (cranial vault), base of skull

A

neurocranium

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4
Q

= face; contains taste, sight and smell organs

A

viscerocranium

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5
Q

The neurocranium forms around the rostral end of the _______

A

neural tube

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6
Q

The viscerocranium forms around the rostral end of the developing _________

A

gut tube

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7
Q

Cartilaginous contributions to neurocranium

A

Cartilaginous (contributes to skull base) → ethmoid, sphenoid, occipital base, petrous temporal, temporal-mastoid

Endochondral ossification (from cartilage)

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8
Q

Membranous contributions to neurocranium

A

Membranous (contributes to cranial vault) → flat bones of vault = parietal, frontal, squamous occipital
Intramembranous ossification
From ossification center, ossify in radial pattern

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9
Q

cartilaginous viscerocranium

A

Malleus, incus, stapes, hyoid, temporal-styloid

Endochondral ossification

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10
Q

membranous viscerocranium

A

premaxilla, maxilla, zygomatic, temporal-squamous, mandible (both)
Intramembranous ossification

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11
Q

fusion of the sagittal suture produces a long front-to-back diameter skull

A

scaphocephaly

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12
Q

= fusion of coronal & lambdoidal sutures bilaterally produces a “tower skull”

A

Turricephaly (oxycephaly, acrocephaly)

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13
Q

fusion of coronal suture bilaterally produces a shortened front-to-back diameter of skull (“flat-head”)

A

brachycephaly

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14
Q

fusion of frontal (metopic) suture producing a median frontal ridge

A

Trigonocephaly

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15
Q

fusion of coronal &/or lambdoidal sutures unilaterally produces an asymmetrical skull

A

plagiocephaly

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16
Q

small head due to a brain that fails to grow

A

microcephaly

17
Q

skull defect the through which the meninges and/or brain herniate.

A

cranioschisis

18
Q

Autosomal dominant genetic disorder characterized by craniosynostosis and other congenital abnormalities e.g., syndactyly of hands and feet, mental retardation.

A

aperty syndrome

19
Q

no skull

A

acrania

20
Q

no brain

A

anencephaly

21
Q

some poorly formed brain stem tissue present

A

meroanencephaly

22
Q

Enlarged ventricles due to too much CSF. If this occurs prior to closure of the sutures, the head enlarges.

A

hydrocephalus