endo Flashcards

1
Q

male pubertal development sequence

A
testicular growth
pubarche
penile growth
spermarche
peak height
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2
Q

female pubertal development sequence

A

thelarche
pubarche
peak height velocity
menarche

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3
Q

delayed puberty age cutoffs

A

girls: 13
boys: 14

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4
Q

premature adrenarche

A

elevated DHEA and DHEA-S
low testosterone

assoc: exogenous androgen, androgen secreting tumor, late onset CAH, PCOS

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5
Q

causes of premature thelarche

A

premature HPA activation
exogenous estrogen
estrogen producing tumor
benign (infants/toddlers - resolves by age 4)

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6
Q

consequence of precocious puberty

A

short adult height

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7
Q

when to use GnRH with precocious puberty

A

<6 yo
male
rapid sx
psychosocial disturbances

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8
Q

inheritance of androgen insensitivity

A

X linked

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9
Q

syndromes assoc with pan hypo pit

A

Prader Willi
Kallmann
septo-optic dysplasia

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10
Q

where does Mullerian inhib factor come from?

A

Y chromosome

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11
Q

male infant with shock and excessive scrotal pigmentation

A

CAH

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12
Q

female infant with shock and posterior labial adhesions

A

CAH

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13
Q

most common cause of CAH

A

21-hydroxylase deficiency
high 17 OHP levels
can have salt wasting variety

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14
Q

cafe au lait spots, bony abnormalities, and endocrinopathies

A

McCune Albright

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15
Q

Cushing Syndrome dx

A

gold standard: 24hr urinary free cortisol excretion
midnight sleeping plama cortisol
dex suppression

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16
Q

DI, exophthalmos, lytic bone lesions

A

Hand Schuller Christian triad of Langerhans Cell histiocytosis
post pituitary involvement

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17
Q

hormones from post pit

A

ADH

oxytocin

18
Q

rate of height growth prior to puberty

A

5-6cm/year

19
Q

micropenis, short stature, hypoglycemia, septo-optic dysplasia, breech presentation

A

congenital GH deficiency

20
Q

calculate mid parental height

A

sum of parents heights
+ 5 if boy, - 5 if girl
divide by 2
+/- 2 inches

21
Q

macrocephaly, cognitive defects, tall stature

A

Sotos syndrome

22
Q

can you mix synthroid with soy formula

A

no - decreases absorption

23
Q

boy with normal TSH and low total T4

A

X-linked thyroxine binding globulin deficiency
dx confirmed with TBG level
no replacement necessary

24
Q

differentiate Hashitoxicosis and Graves

A

radioiodine uptake - high in Graves, low/normal in Hashi

25
tx Hashimoto
lifelong levothyroxine
26
tx Graves
methimazole no PTU surgery if methimazole ineffective
27
tx neonatal thyrotoxicosis
methimazole until maternal Abs cleared
28
constipation, fatigue, muscle weakness
hypercalcemia
29
causes of hypercalcemia
Williams ingestion (vitamin D, A, thiazides) skeletal disorders/immobilization hyperparathyroidism
30
tx hypercalcemia
fluids, lasix, EKG
31
muscle spasms, vomiting, seizures resistant to benzos
hypocalcemia | can have prolonged QT
32
causes of hypocalcemia
``` pseudohypoparathyroidism (PTH resistance) nutritional DiGeorge nephrotic syndrome renal ```
33
hypocalcemia and hyperPh
hypoPTH
34
hypercalcemia and hypoPh
hyperPTH
35
hypocalcemia and hypoPh
vit D deficiency
36
hypocalcemia resistant to Ca replacement
think about mag
37
bone pain, growth delay, widening of joint spaces
Rickets | serum alk phos ALWAYS elevated
38
causes of vit D deficient Rickets
``` BF w/o supps no sun exposure low BW/prematurity vegan diets liver disease --> poor absorption ```
39
low Ca, normal 25-OH vit D, low 1,25-OH vit D
vit D dependent rickets AR inadequate renal prod of activated vit D
40
tx vit D dependent rickets
D2 and 1,25 vit D
41
low Ph, low Ca, high alk phos, high PTH, high 1,25 vit D
hereditary vitamin D resistant rickets end organ resistance AR
42
low Ph, normal Ca, high alk phos, normal PTH, normal vit D levels
X linked hypophosphatemic rickets XL dominant tx: 1,25 vit D and phos