Infant Disorders Flashcards

1
Q

CL occurs in

A

1 in 700 births

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2
Q

CL is a str or fx prob

A

str

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3
Q

What problem occurs embryonically in CL? When does this occur?

A

maxillary and nasal sinuses do not fuse

Week 5-8 gestation

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4
Q

CL: uni or bilateral?

A

Either

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5
Q

What teratogens play a role in CL? Examples of positive/negative?

A

Positive: smoking, viral infections
Negative: folic acid deficiency

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6
Q

Why does CL usually occur w CP?

A

The teratogen present in week 5-8 for CL usually has not gone away by week 9-12 for CP

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7
Q

How often does CP occur?

A

1 in 2000

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8
Q

Brief description of CP

A

congenital, incomplete fusion of palatine structures at week 9-12

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9
Q

What is the strongest Et factor in CP?

A

smoking during pregnancy

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10
Q

How often does pyloric stenosis occur?

A

1 in 1000

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11
Q

Is pyloric stenosis congenital/genetic?

A

No

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12
Q

Is pyloric stenosis a structural or functional problem?

A

functional

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13
Q

Why is there constriction of the pyloric spinster in pyloric stenosis?

A

Hypertophy

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14
Q

Et of pyloric stenosis

A

hypergastrinemia, PGE, erythromycin exposure

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15
Q

PGE is…

A

a local hormone

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16
Q

When does pyloric stenosis occur?

A

2-8 weeks of AGE

17
Q

How does obstruction occur in pyloric stenosis

A

hypertrophy of sphincter = constriction = inflammation/exudate formation = obstruction

18
Q

manifestation of PS?

A

projectile vomiting

19
Q

What are 2 complications of PS?

A

dehydration, malnourishment

20
Q

Diagnostic confirmation of PS?

A

URQ palpation = mass felt

21
Q

How do we treat PS?

A

sx to debulk muscle

22
Q

What kind of problem is gastroesophageal reflux?

A

functional and neuro prob

23
Q

How often does gastroesophageal reflux occur in infants? When does it subside?

A

50%. After 3 months

24
Q

Et of gastroesophageal reflux?

A

neuromuscular

25
Q

Why do growth problems occur in gastroesophageal reflux?

A

pain during feeding, so baby doesn’t want to feed

26
Q

tx for gastroesophageal reflux?

A

H2RA, antacids, PPI, modify feeding (positioning, smaller feeds, thickened), fundoplication

27
Q

Et of Hirschsprung Disease?

A

RET gene on Chr 10 = codes for proteins involved in cell signalling, helps in formation of neural tissue in colon

28
Q

Patho of Hirschsprung Disease

A

areas of colon lack PS ganglia = no peristalsis in that area = accumulation of contents = colon distension = abdominal distention

29
Q

How do we treat Hirschsprung Disease

A

sx removal of aganglionic segment

30
Q

How often does intussusception occur?

A

1 in 4000

31
Q

What happens in intussusception?

A

Intestines invaginate into adjoining valve

32
Q

What adjoining valve do intestines usually invaginate into in intussusception?

A

Ileocecal valve

33
Q

Why does this invagination occur?

A

Region of smaller diameter is pushed into one with a larger diameter due to pressure build up

34
Q

How do we treat intussusception?

A

hydrostatic reduction