Endocrine Flashcards

1
Q

fetal thyroid production depends on the mother’s ____ levels for its thyroid hormone synthesis

A

iodine

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2
Q

Thyroid is from what layer in development? What pharyngobronchial pouch?

A

endoderm
4th pharyngobronchial pouch

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3
Q

what thyroid hormone does NOT cross placenta

A

TSH

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4
Q

Fetal T3 and T4 and TSH and transition after birth

A

T4 rise after 20 weeks
T3 rise after 30 weeks (thyroid gland can convert T4 to T3 by this time)

TSH surge (due to COLD) after birth
along with T3 and T4.

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5
Q

if baby has congenital hypothyroidism (1:3000-4000) live birth, what other congenital defect you need to think about

A

slightly increase in congenital heart defect (5.2-9% while general population 2.5-9%)

2% w/ family hx.

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6
Q

if free T4 is normal, but T4 total is low, this means there are low total thyroid hormon but also low binding TBG. so enough free T4 to function.

A
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7
Q

anterior pituitary gland from where
posterior pituitary gland from where

A

Rathke’s Pouch (adenophypophysis)

3rd ventricle (ectoderm, neurohypophysis)

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8
Q

hCG stablize SRY

A
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9
Q

CAH is what genetic pattern

A

all Autosomal RECESSIVE.

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10
Q

when can you clear salt wasting crisis (by what DOL)

A

day 10

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11
Q

5 alpha reductase deficiency

A

no testicular descend, at beginning

but age 12, more testosterone, –> become boy.

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12
Q

how to tell difference between CAH baby and pseudohypoaldosteronism

A

Both have salt wasting, high K, and low BE.

Pseudohypoaldosteronism has HIGH Aldosterone.
But CAH has limited Aldosterone

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13
Q

An infant of a diabetic mother has hypocalemia secondary to

A

Reduced transplacental transfer of calcium secondary to increased urinary excretion of Ca2+ and Mg2+

Mom pees more due to hyperglycemia

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14
Q

if baby has low Ca, also need to replace what electrolyte

A

Mg

Mg is needed for PTH release
(but too much Mg, hyperMg, can inhibit Ca influx at the neuromuscular jxn leading to decrease tone in neonate)

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15
Q

Pseudohypoparathyroidism gene pattern

A

AD

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16
Q

somatostatin is the second line after Diazoxide . why?

A

mutation in K-ATP channel, then not responding to diazoxide.
somatostatin can act on Ca channel of some sort.

17
Q

insulin and ketone

A

excess insulin –> NO ketone. (glucose drive into cells)

18
Q

what enzyme is deficient in Galactosemia

A

Galactose 1-phosphate uridyl transferase deficiency

19
Q

Wolcott - Rallison syndrome (AR)

A

cardiac, hepatic, renal anomalies
Diabetes Mellitus
Multiple epiphyseal/spondyloepiphyseal dysplasia

20
Q

Neonatal Diabetes

A

In sulfonylurea receptor (Tx with high dose sulfonylurea)

Genetic defect (KCNJ11; ABCC8)
treated with sulfonylurea once mutation is known.

Signs and symptoms
−IUGR
−Dehydrated
−Poor weight gain
−Hyperglycemia

21
Q

hypoparathyrodism Lyte patter

A

hypocalcemia
hyperphosphatemia

22
Q

neurogenic DI vs. nephrogenic DI

A

Neurogenic DI: not making enough ADH (ADH made in hypothalamus)
Nephrogenic DI: make enough ADH but kidney not responding to ADH