Molecular Genetics and Early Embryonic Development & Craniofacial Conditions Flashcards

1
Q

In every species and at every level of organization, complex structures are made by repeating a few basic _____ with variations.

A

themes

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2
Q

_____: cells begin to form specific and specialized structures

A

Differentiation:

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3
Q

_____: cell divisions that form more cells with identical functions as the parental cell

A

Growth:

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4
Q

______: cells produced by cleavage get organized into layers and groups of cell masses through what is known as gastrulation.

A

Patterning

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5
Q

Patterning needs to occur in what 3 dimensions?

A

–Anterior-Posterior (top-bottom)
–Dorsal-Ventral (left-right)
–Proximal-Distal (front-back)

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6
Q

During what weeks of development do the craniofacial structures develop?

A

3-8 weeks

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7
Q

What are the 5 main signaling pathways involved in development?

A
Receptor tyrosine kinase
TGFB
Wnt
Hedgehog
Notch
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8
Q

____ division: sister cells are born different

A

Asymmetric divison

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9
Q

______ division: sister cells become different as result of influences acting on them after their birth

A

Symmetric division

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10
Q

What percentage of all live births exhibit some form of minor or major abnormality?

A

3%

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11
Q

Embryonic cell population that is localized between the developing neural tube and the epidermis.

A

Neural crest cells

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12
Q

Some neural crest cell exhibit _____ in that they can give rise to multiple differentiated cell types

A

“stemness”

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13
Q

In the formation of the craniofacial structures (and many other structures) the _______ migrate through restricted pathways to form the developing structures.

A

neural crest cells

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14
Q

Cell migration is a tightly regulated processes and the ____ receive cues such as morphogens and growth factors that restrict their movement and determine fate

A

neural crest cells

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15
Q

Over ____ genes identified that have mutations associated with tooth patterning, morphogenesis defects and cell differentiation defects

A

300

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16
Q

As a collective group ______ diseases are the most common

A

craniofacial genetic

17
Q

–>100 different disorders

–Commonly involves one or more of teeth, nails, skin, sweat glands and/or hair

A

Ectodermal dysplasias

18
Q

_____: common types of tooth agenesis with only a few missing teeth

A

Hypodontia:

19
Q

_____: more severe form of tooth agenesis with at least 6 missing teeth, excluding third molars

A

Oligodontia

20
Q

_____: complete lack of teeth

A

Anodontia

21
Q

_____: one or more teeth appear smaller

A

Microdontia

22
Q

_____: one or more teeth grow faster and exceed average size

A

Macrodontia

23
Q

What are the most common craniofacial conditions?

A

Cleft lip and palate

24
Q

What 2 processes fail to fuse in cleft lip/palate?

A

medial nasal and maxillary processes

25
Q

_____ provide support for erupting teeth and orthodontic tooth movement

A

Alveolar bone graft

26
Q

What are the 3 things that make up the Robin sequence?

A

Glossoptosis
Micrognathia
Respiratory distress

27
Q

What is the gold standard treatment for Pierre-Robin syndrome?

A

Neonatal mandibular distraction

28
Q

____ is a surgical technique in which new bone formation is induced by gradual separation of bony segments after osteotomy

A

Distraction osteogenesis