Folding, Body Partitions, and Lateral Folding Flashcards

1
Q

What partition separates the thoracic cavity from the abdominal cavity?

A

diaphragm

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2
Q

What four subcomponents define the diaphragm?

A

septum transversum, pleuropotential membranes, dorsal mesoderm, esophageal mesoderm

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3
Q

When is the embryonic stage of lung development?

A

4-7 weeks

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4
Q

When is the pseudoglandular stage of lung development?

A

5-17 weeks

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5
Q

When is the canalicular stage of lung development?

A

16-25 weeks

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6
Q

When is the terminal sac stage of lung development?

A

24 weeks - birth

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7
Q

When is the alveolar stage of lung development?

A

8 months - 8 years

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8
Q

What defines the embryonic stage of lung development?

A

lung buds, lung lobes, bronchopulmonary segments

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9
Q

What defines the pseudoglandular stage of lung development?

A

lung looks like a gland, all major passages are present except those for gas exchange

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10
Q

What defines the canalicular stage of lung development?

A

enlargement of bronchi and bronchioles, terminal sacs present by end of period, surfactant is present by 20 weeks (not enough)

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11
Q

What defines the terminal sac stage of lung development?

A

terminal sacs multiply, lining thins, capillarity increases, there is enough surfactant to prevent lung collapse

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12
Q

What defines the alveolar stage of lung development?

A

terminal sacs continue to differentiate to alveolar ducts;
birth - 3 years
increase in number of alveoli and respiratory bronchioles
3-8 years
increase in number and size of alveoli

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13
Q

What is the respiration rate of newborns? Adults?

A

40-80/min, 12-18/min

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14
Q

What is tracheal esophageal fistula?

A

esophageal atresia, extra amniotic fluid, fluid doesn’t reach intestine

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15
Q

What is congenital diaphragmatic hernia?

A

failure in diaphragm precursors to properly fuse, leading to malformation of lungs and heart as GI contents invade

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16
Q

What is respiratory distress syndrome?

A

lack of surfacent which reduces surface tension and prevents collapse; can lead to detachment of alveolar lining

17
Q

SIDS

A

insufficient development of medulla respiratory control centers

18
Q

cystic fibrosis

A

faulty gene leads to abnormal Cl channels; less Cl exits, less water follows; thick mucous clogs lungs, liver, and pancreas