Endocrinology Flashcards
solitary maxillary central incisor indicates high likelihood of __ deficiency
GH deficiency
Prolactin is (low/high) in hypothyroidism
HIGH because TRH is increased which inhibits production of DA from hypothalamus
Constitutional growth delay:
growth velocity?
bone age?
fam hx?
NORMAL growth velocity
DELAYED bone age
+ Fam Hx of delayed puberty
Diagnosis of DI
Clinical: polyuria, polydipsia, chronic dehydration
Urine: pale, colorless, Osm <300, SG <1.010
Dx via water deprivation test of giving DDAVP
SIADH:
serum NA?
serum Osm?
urine Osm?
urine volume?
ADH?
atrial natriuretic peptide?
HYPOnatremia
LOW serum Osm
HIGH urine Osm
LOW urine output
HIGH serum ADH
NORMAL atrial nat peptide
What causes SIADH?
pna,t umor, TB, CF, meningtiis, head trauma
What causes hyponatremia in ICU setting?
SIADH vs cerebral salt wasting (caused by CNS disorders such as tumor, CVA, head trauma, hydrocephalus)
What will you see with cerebral salt wasting?
serum NA?
serum Osm?
urine Osm?
urine volume?
ADH?
atrial natriuretic peptide?
HYPOnatremia
LOW serum Osm with HYPOvolemia
HIGH urinary Na excretion
INCREASED urine output
LOW vasopressin
HIGH atrial peptide
what causes cerebral salt wasting?
what is treatment?
hypersecretion of atrial natriuretic peptide
Replacement of urine output with IV fluids (NS to 3% saline)
What is inheritance pattern of these disorders that cause tall stature?
- Klinefelter syndrome
- Marfan’s
- homocystinuria
- XXY
- AD
- AR
Marfan syndrome has (up/down) lens subluxation and (up/down) IQ.
Marfan: UP/UP
Homocystinuria: Down/Down
What is Sotos syndrome (aka cerebral gigantism)
- Infants born >90th% and grow rapidly in 1st year of life to >97th%
- Growth continues for 4-5yrs, then returns to normal rate
- children have big hands/feet and are clumsy
- most end up with normal height
- GH levels are NORMAL! (this is NOT an endocrine d/o)
How would an adolescent female present with prolactinoma?
- HA
- Amenorrhea
- galactorrhea (milk from breasts)
- visual-field defects
- Usually presents after puberty
What is Beckwith-Wiedemann syndrome?
- fetal overgrowth with organ hypertrophy
- macroglossia, HSM, nephromegaly
- pancreatic B-cell hyperplasia (hypoglycemia)
**predisposed to WIlms tumor, adrenocortical carcinoma, and hepatoblastoma
- need to follow with abd U/S every 3mo until age 8 and AFP every 6wks until age 6
What hormone is reponsible for initiation of puberty?
GnRH