embryology of endocrine system Flashcards

(49 cards)

1
Q

timeline of development of endocrine glands

A

weeks 3-8

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2
Q

Rathkes pouch

A

invagination of oral cavity

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3
Q

Rathkes pouch will become

A

anterior pituitary

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4
Q

infundibular stalk comes from what and becomes

A

invagination of diencephalon called the neurohypophyseal diverticulum, posterior pituitary

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5
Q

adenohypothysis (anterior lobe of pituitary) contains what

A

pars anterior
pars tuberalis
pars intermedia

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6
Q

neurohypophysis (posterior lobe) contains what

A

pars nervosa
infundibular stem
median eminance

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7
Q

hormone release process in pituitary

A

made in anterior lobe and released by posterior lobe

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8
Q

anterior lobe function

A

hypothalamic hormones are carried through the hypophyseal portal veins to the anterior pituitary, regulating secretion of trophic hormones

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9
Q

ADH function

A

production and concentration of urine

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10
Q

oxytocin function

A

important near term of pregnancy, allow uterine contractions
important for lactation

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11
Q

craniopharyngiomas

A

most common pituitary tumor in children and adolescents

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12
Q

what is a craniopharyngioma

A

benign epithelial tumor arising from remnants of rathkes pouch
can be supra sellar or intra sellar (sella turcica)

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13
Q

symptoms of craniopharyngiomas

A

vision loss, diabetes insipidus

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14
Q

intrasellar cystic craniopharyngiomas route of surgical removal

A

intra nasal

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15
Q

suprasellar craniopharyngiomas info and route of surgical removal

A

grown within 3rd ventricle and can cause hydrocephalus
frontotemporal removal

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16
Q

pituitary adenoma effects

A

growth hormone production causing the liver to make IGF1
can cause body size changes

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17
Q

pituitary adenoma develops before epiphysis is fused

A

gigantism

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18
Q

pituitary adenoma forms after epiphysis is fused

A

growth in nose, hands, feet, maybe mandibular defects

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19
Q

superior parathyroid gland develops from which pharyngeal pouch

A

pouch 4

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20
Q

inferior parathyroid gland develops from which pharyngeal pouch

21
Q

cell types of parathyroid glands

A

chief cells present at birth secrete PTH and sense low calcium
oxyphil cells appear at puberty

22
Q

DiGeorge syndrome caused by

A

deletion of chromosome 22q and TBX1 gene
failure of pharyngeal pouches 3 and 4 to differentiate into thymus and parathyroid gland

23
Q

clinical features of DiGeorge

A

immunodeficiency
hypocalcemia
cardiac abnormalities- tetralogy of fallot
abnormal jaw
thymus aplasia
cleft palate
hypocalcemia and hypoparathyroidism

24
Q

what is the derivative of the thyroid gland

A

not a pouch, the floor of pharynx

25
ultimobranchial body derives from
pharyngeal pouch 4
26
thyroid gland function begins when
week 10
27
C- cell function and derivative
produce calcitonin and derived from endoderm
28
aberrent locations of thyroid tissue is caused by
abnormal migration of thyroid glands part of thyroglossal duct can persist and form a cyst
29
congenital hypothyroidism causes
the most common cause of mental delay and can be prevented and treated
30
causes of congenital hypothyroidism
thyroid dysgenesis nonfunctioning goiters central hypothalamic or pituitary hypothyroidism
31
untreated congenital hypothyroidism causes
failure of skeletal growth and maturation and deficiency in intellect
32
dorsal pancreas is formed by
out pouching of duodenum
33
what allows pancreatic hormones to be made
the suppression of sonic hedgehog in that area of duodenum
34
ventral pancreatic bud forms off of
common bile duct
35
ventral duct persists as main pancreatic duct (proximal) and attaches where
major duodenal papilla
36
pancreas and duodenum are
secondary retroperitoneal
37
gestational diabetes causes
high maternal glucose
38
effect of gestational DM on baby
maternal glucose can cross placenta but insulin cannot- increased fetal growth - fetal hyperinsulinemia and increase in fetal fat cells
39
normal pregnancy glucose levels
first trimester: decrease in fasting plasma glucose concentration second and third trimester: increase in plasma glucose concentration - promotes fat breakdown
40
congenital hyperinsulinism effects
diffuse B-cell hyperplasia and intractable hypoglycemia - high levels of insulin due to issues with pancreas
41
hyperinsulinemia
higher levels of insulin without a problem with pancreas
42
lateral urogenic ridge becomes
kidneys
43
gonadal ridge cells delaminate via what to form what
EMT to form fetal adrenal cortical cells, the adult version forms via a second wave
44
precursors of chromafin cells
neural crest cells
45
adult and fetal adrenal cortical cell origin
intermediate mesoderm
46
deficiency In 21-hydroxylase causes which electrolyte changes and sexual traits
hyponatremia, hyperkalemia and ambiguous genitalia in females
47
deficiency In 11B-hydroxylase causes which electrolyte changes and sexual traits
hypernatremia and hypokalemia ambiguous genitalia in females
48
deficiency In 17a-hydroxylase causes which electrolyte changes and sexual traits
hypernatremia, hypokalemia and ambiguous genitalia in males
49
pheochromocytoma secrete what and cause what
secrete catecholamines that arise from chromaffin cells, causing hypertension curable by removal of tumor