1.8.15 - Endocrine Cases Flashcards

1
Q

systemic sluggish reflexes

A

diabetes

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2
Q

treatment of chapmans

A

anterior point
posterior point
then recheck anterior point

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3
Q

sympathetics to thyroid

A

vasomotor

T1 - often flexed

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4
Q

cervical ganglia

A

superior
middle
inferior

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5
Q

superior cervical ganglion

A

C2-3

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6
Q

middle cervical ganglion

A

C6 transverse process

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7
Q

inferior cervical ganglion

A

C7 and rib

aka stellate

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8
Q

VSR

A

more rubbery end feel

-no HVLA usually

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9
Q

abdmonial ganglia

A

celiac
SMA
IMA

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10
Q

focus on treating SD

A

don’t chase the pain

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11
Q

labs for hypothyroid

A

TSH and free T4

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12
Q

liver

A

activates T4 > T3

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13
Q

TSH repeat

A

6 weeks untils table

6-12 months once stable

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14
Q

sleep apnea

A

predispose for heart disease

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15
Q

metabolic syndrome diagnosis

A

3 of 5

1 - abdominal obesity
men >102cm
women >88cm
2 - BP >130/85
3 - TG > 150
4 - HDL - men 100
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16
Q

adrenal fatigue

A

subclinical addisons disease

17
Q

ketoconazole, etomidate

A

possible etiology of addisons

18
Q

low cortisol and high ACTH

A

addisons disease

normal cortisol - adrenal fatigue

19
Q

adrenal crisis

A

5 S’s

salt, sugar, steroids, support, and search (for precipitating illness)

20
Q

tx of addisons

A

managed with hydrocortisone, fludrocortisone, and DHEA

21
Q

in utero

A

growth depends on maternal factors

22
Q

after birth

A

growth depends on genetics

23
Q

first 18 months

A

catch up or catch down growth

before reach genetic growth velocity

18-24 months - kids grow along same percentile

24
Q

constitutional delay of growth and puberty

A

temporary delay of growth but catch up mid puberty

25
Q

growth failure

A

loss of two or more major percentile lines

26
Q

short stature

A

height 2 SD below average

or below 2.5 percentile

27
Q

familial short stature

A

short compared to age matched population but consistent with family genetics

28
Q

non-familial short stature

A

short compared to population and family

29
Q

history with short stature

A

pregnancy/birth history
fam hx
previous growth

30
Q

webbed neck, low ears, broad chest

A

turner syndrome

31
Q

webbed neck, double curve scoliosis, rib deformity

A

noonan syndrome

32
Q

triangular face, clinodactyly, blue sclera, lack of subQ fat

A

russel silver

33
Q

multiple fractures, missing collar bone, underdeveloped joints

A

skeletal dysplasia

34
Q

lab for short stature

A
BMP
CBC
ESR
LFT - liver function test
urinalysis
bone age and Xray - left hand and wrist
35
Q

multiple syndromic or dysmorphic features

bone age <2SDs

A

referral indicated

36
Q

GH stimulation test positive

A

GH deficiency

tx GH injection to puberty

37
Q

somatosensory mapping

A

develop through motion

best time to influence biomechanics and somatosensory map
-just before growth spurts

38
Q

common compensatory pattern

A

??