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42 Cards in this Set
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Addisons description
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adrenal secretes too little cortisol, aldosterone, or both. TB used to be most common. autoimmune now most common. along with thyroid, parathyroid.
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Addisons sx
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chronic, progressive muscle weakness, malaise, anorexia, weight loss, GI, hyperpigmentation.
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Addison labs
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hypoglycemia, hyponatremia, hperK, acidosis.
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Addisonian crisis
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rapid adrenal destruction (adrenal hemorrhage), or when compensated patient has stress. needs fludrocortisone (mineralocorticoid), and hydrocortisone (glucocorticoid).
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Turner syndrome features
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1 :2000 girls. small stature, gonad dysgenesis. cardiac (bicuspid aorta), coarct, aortic stenosis, MVP. HTN. Renal abnormalities
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low T4, elevated TSH, slowed growth
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acuquired hypothyroidism. chronic lymphocytic thyroiditis (Hashimoto). female > male.
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congenital hypothyroidism
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coarse face, puffy eyelids, thick tongue, thick hair. splayed sutures.
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sudden change of growth at 5yrs old, becomes fat and short.
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Cushing or hypothyroidism.
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Cushing S
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most commonly exogenous steroids.
growth stops, become fat. central obesity, hypertension, buffalo hump, hirsutism, striae, acne. |
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hypothyroidism growth changes
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weight loss and increased growth velocity is more common. can become short and fat however.
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hypercalcemia in the immobilized
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decreased bone mineralization due to no weight bearing causes Ca excess.
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familial short stature
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normal PE except short and small. nl birthweight. become short within first 2yrs.below but parallel to 5th percentile. bone age = chronologic age. Differs from
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congenital adrenal hyperplasia, salt wasting
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ambiguous genitalia, low salt, hi K, hi 17-hydroxyprogesterone.
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hyperthyroid sx
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tachycardia, weight loss, exophthalmos, remor. emotional labitility.
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precocious puberty def.
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signs of puberty before 8 in girl, 9 in boy.
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work up of precocious puberty
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bone age. Nl: incomlete sexual precocity. delayed bone age - hypothyroidism. advanced bone age - true precocious puberty vs pesudocomplete. (use CT for that)
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hypoparathyroid sx
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seizure from hypocalcemia. hi phosphate, nl Mg, low parathyroid hormone.
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DiGeorge sx
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cell mediated immune d. hypoparathyroidism. face, CV anomalies
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DiGeorge heart
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truncus, aortic arch anomalies.
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hyperthyroidism sx
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weight loss, impulsivity, inattentiveness, emotional lability. lid lag, jittery, tremor, tachy, sweating.
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hypoparathyroid does what to Ca
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low Ca, hi Phos
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how to differentiate GH deficiency from constitutional growth delay.
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GH deficiency falls off curve in height. Constitutional is always trachking below 5th, but gaining. both have delayed bone age. FH of growth or puberty delay. familial short stature: normal linear tgrowth, bone age = chrono,
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thyroid binding globulin deficiency dx
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clinically euthyroid, normal growth. low T4, nl TSH, hi T3 resin
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hypocalcemia in neonate
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nl is 7-10 with iCa 1.0. Most common hypoCa is due to prematurity.
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changes to external genitalia of term infant caused by what hormones
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androgens alone cause external genitalia to change.
estrogens may cause withdrawl bleed, lactation |
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pubertal gynecomastia diff
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often start unilat, most become bilat.
Klinefelters: tall, small testes. testicular carcinoma: secrestes estrogens, mass lipomas, usually not beneath areola. obese patients have adipose tissue, no breast tissue. |
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Turner s. sx
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primary amenorrhea. short, norm weight, no breast tissue (ovaries not working), normal pubic hair (androgens working)
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Graves D. dx sx
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big thyroid, hyper thyroid: weight loss, poor school performance, poor concentration, nervousness, heat intol. tachycardia, tremorT4 hi, TSH lo
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simple goiter
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big thyroid, euthyroid
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thyroid nodule
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discrete nodule. Refer all to ped endo to R/O malig
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treatment of Graves
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methimazole, carbimazole, or propylthiouracxil. suppress for 1-2 yrs, if fails then do radioI, if that fails then cut it out.
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neonatal hyperthyroidism
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due to transplacental TSH receptor stimulating Ab from mother with Graves. irritabale, jittery, tremulous, flushed, sweating, exopth, HS meg. tachy.
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hypophosphatemia
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Rickets is any disease of bones due to low phostphate or Ca. Xr hypophosphatemic rickets is most common inheritied rickets. renal wasting of phosphate.
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21 hydroxylase deficiency sx
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ambiguous genitalia in girl
75% have aldosterone def. = salt wasting presenting in 2nd week.. FTT, vomit, with hyperpigmentation (ACTH overproduction) |
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age by which height percentile stabiliizes
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3yrs. significant decreases after should be investigated.
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growth pattern: constitutional delay of growth and puberty.
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nl birth. slow linear growth or decrease in first 3years of life. FH of late bloomer. bone age delayed to height age.
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familial short stature
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similar start as constitutional but bone age matches chrono. final height appropriate to parents.
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short child with incrased weight to height ratio
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think endocrine: GHD. either congenital septooptc dysplaisa or very rare defect in ACTH gene
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short and dysmorphic
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Down, Turner, Noonans, Prader-Willi
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endocrine causes of short stature
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thyroid def or resistance
Cushings S congenital adrenal yperplasias too much steroids neuroendocrine GH disorders |
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single central incisor, think
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GH deficiency
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pale optic disk, think
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septo-optic dysplasia.
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