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70 Cards in this Set
- Front
- Back
Where are the Islets of Langerhans most numerous?
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Tail of the pancreas
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Effect of insulin on the kidney?
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Increase Na+ reabsorption
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Cells that DON'T need insulin for glucose uptake?
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Brain
RBC Intestine Cornea Kidney Liver |
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Cells that use GLUT1 transporter?
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Brain and RBCs
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Cells that use GLUT2 transporter?
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Beta islet cells
Liver Kidney Small intestine |
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Embryological origin of anterior and posterior pituitary?
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Anterior: oral ectoderm (Rathke's pouch)
Posterior: neuroectoderm |
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Where do neurophysins work?
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They carry proteins of hormones from the hypothalamus to posterior pituitary.
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Embryological origin of adrenal cortex and medulla?
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Adrenal cortex: mesoderm
Adrenal medulla: neural crest |
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The same alpha subunit is shared by which hormones?
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TSH
LH FSH hCG |
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Somatostatin mainly inhibits what 2 hormones from the pituitary?
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GH and TSH
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Cause of apparent mineralocorticoid excess?
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Deficiency or inhibition of 11-beta-HSD2 (normally degrades cortisol to cortisone)
--> cortisol is able to bind to MR and act like aldosterone |
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2 compounds that osteoblasts produce?
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M-CSF and RANK-L
Production of both is increased by PTH. |
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Cause and effect of low Mg on the endocrine system?
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Causes: diarrhea, AGs, diuretics, alcohol
Effect: low Mg decreases PTH secretion |
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Effect of PTH on osteoblasts and osteoclasts?
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Directly stimulates osteoblasts (which indirectly stimulates osteoclasts).
Also directly stimulates osteoclasts. --> Enhances bone matrix degradation |
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Causes of low phosphate?
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Low Vitamin D
Insulin (phosphorylated glucose) Primary hyper-PTH PTHrP Metabolic/resp alkalosis (activate PFK) Vitamin D-resistant rickets |
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What increases in the urine with PTH stimulation?
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Urine (PO4)3-
Urinary cAMP |
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Breakdown of total body Ca?
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40% bound to albumin
Some bound to phosphate 13% bound to citrate 47% free/ionized |
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Effect of high and low levels of SHBG in men vs women?
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Men: high levels --> lower free testosterone --> gynecomastia
Women: low levels --> higher free testosterone --> hirsutism |
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Testosterone in blood?
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1-2% free
30-50% bound to albumin 40-50% bound to SHBG |
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Where is most T3 formed?
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In the blood
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3 causes of decreased TBG levels?
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Hepatic failure
Anabolic steroid use Nephrotic syndrome |
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Hormone with nuclear receptors?
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T3/T4
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Hormones that use receptor-associated tyrosine kinase (JAK/STAT pathway)?
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GH and prolactin
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Hormones that use intrinsic tyrosine kinase (MAP kinase pathway)?
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Insulin, IGF-1, FGF, PDGF
^^ Growth factors |
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Hormones that work through IP3 pathway?
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GnRH, Oxytocin, ADH (V1), TRH
"GOAT" |
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Hormones that work through cGMP pathway?
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ANP, NO (EDRF)
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Hormones that work through cAMP pathway?
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FSH, LH, ACTH, TSH, CRH, hCG, ADH (V2), MSH, PTH
+ calcitonin, GHRH, glucagon "FLAT CHAMP" + CGG |
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Risks for Waterhouse-Friderichsen syndrome?
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Neisseria meningitidis septicemia
DIC (or anti-coagulation) Endotoxic shock (or hypotension) |
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Primary vs secondary Addison's disease?
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Primary: due to adrenal atrophy or destruction by disease (aldosterone AND cortisol deficiency)
Secondary: decreased ACTH production (low cortisol, normal aldosterone) |
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Polyglandular autoimmune syndrome (PAS) type I?
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Addison's
Primary hypo-PTH Mucocutaneous candidiasis Autosomal recessive, in kids |
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Polyglandular autoimmune syndrome (PAS) type II?
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Addison's
Hashimoto's Type I DM Autosomal dominant, in adults, associated with HLA DR3/4. |
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What condition is opsoclonus-myoclonus syndrome is associated with?
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Neuroblastoma
Affects 2-3% of pts |
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Pheochromocytomas are associated with what other conditions?
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Neurofibromatosis
MEN IIa MEN IIb |
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Symptoms (5 P's) of pheochromocytoma?
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Perspiration
Pain (headache) Palpitations Pressure (HTN) Pallor |
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Breakdown of NE by MAO produces what? COMT?
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NE
--> MAO --> VMA --> COMT --> normetanephrine |
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Secondary causes of hyperaldosteronism?
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Renal artery stenosis
Chronic renal failure CHF Cirrhosis Nephrotic syndrome |
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Change in lab values with hyperthyroidism?
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Increased glu, Ca, lymphocytes
Decreased cholesterol |
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Bone pain with cystic bone spaces filled with brown fibrous tissue?
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Osteitis fibrosa cystica
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What is Chvostek's sign?
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Tapping of facial nerve causes contraction of facial muscles
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Occlusion of brachial artery with BP cuff causes carpal spasm. Sign?
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Trousseau's sign
Sign of hypocalcemia |
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Cause and findings in pseudohypo-PTH (Albright's hereditary osteodystrophy)?
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Cause: autosomal dominant kidney unresponsiveness to PTH
Findings: hypocalcemia, short 4th/5th digits, short stature |
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Histology of thyroid gland in Hashimoto's?
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Hurthle cells with lymphocytic infiltrate with germinal centers
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Endemic vs sporadic cretinism?
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Endemic: iodide deficiency
Sporadic: defect in T4 formation or thyroid developemental failure |
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Findings in cretinism (5 P's)?
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Pot-bellied
Pale Puffy-faced Protruding umbilicus Protuberant tongue |
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Subacute painful vs painless thyroiditis?
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Painful: de Quervain's (follows flu-like illness)
Painless: lymphocytic, autoimmune/post-partum |
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Findings in de Quervain's thyroiditis?
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Elevated ESR
Jaw pain Early inflammation Very tender thyroid |
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Jod-Basedow phenomenon?
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Thyrotoxicosis if a patient with iodine deficiency goiter is made iodine replete
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Medullary thyroid cancer histology?
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Sheets of cells in amyloid stroma
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4 findings in diabetic retinopathy?
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Hemorrhage
Exudates Microaneurysms Vessel proliferation (VEGF) |
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Histology of type 1 vs type 2 DM?
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Type 1: islet leukocytic infiltrate (insulitis)
Type 2: islet amyloid deposit |
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Aldosterone level in SIADH?
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LOW (body tries to maintain near-normal volume)
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Causes of central DI?
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Pituitary tumor
Trauma Surgery Histiocytosis X |
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Treatments for nephrogenic DI?
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Hydrochlorothiazide
Indomethacin Amiloride |
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Common presentation of MEN I?
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Kidney stones and stomach ulcers
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Inheritance of MEN syndromes?
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All are autosomal dominant
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Where is tumor located in Zollinger-Ellison syndrome?
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Pancreas or duodenum
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Rule of 1/3s for carcinoid syndrome?
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1/3 metastasize
1/3 present with 2nd malignancy 1/3 multiple |
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Complications of DKA?
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Life threatening mucormycosis/Rhizopus
Cerebral edema Cardiac arrhythmias Heart failure |
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Drug to control uterine hemorrhage?
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Oxytocin
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Specific toxicities of Propylthiouracil vs Methimazole?
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PTU: hepatotoxic
Methimazole: teratogenic Both can cause skin rash, agranulocytosis, and aplastic anemia. |
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Rapid, intermediate, and long acting insulins?
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Rapid: Lispro, Aspart, and Regular
Intermediate: NPH Long: Glargine, Detemir |
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Which diabetic drug can cause pancreatitis?
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Exenatide (GLP-1 analog)
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Action of Pramlintide (amylin mimetic)?
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Decrease glucagon release
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Mechanism of Acarbose and Miglitol?
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Alpha-glucosidase inhibitors
(inhibit intestinal brush border enzymes that hydrolyze sugars --> decreased glucose absorption) |
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Diabetic agents that bind PPAR-gamma?
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Glitazones/thiazolidinediones:
- Pioglitazone - Rosiglitazone |
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1st vs 2nd generation sulfonylureas?
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1st gen: Tolbutamide, Chlorpropamide
2nd gen: Glyburide, Glimepiride, Glipizide |
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AE of 1st vs 2nd generation sulfonylureas?
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1st gen: disulfiram-like effects
2nd gen: hypoglycemia |
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17-OH-progesterone levels in each congenital adrenal hyperplasia?
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Increased in: 21-hydroxylase and 11-beta-hydroxylase deficiency
Decreased in: 17-alpha-hydroxylase deficiency |
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11-deoxycorticosterone (DOC) is a precursor to what and is elevated in what condition?
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Precursor to aldosterone. It has mineralocorticoid activity.
Elevated in 11-beta-hydroxylase deficiency. |
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17-hydroxy-corticoids refer to what?
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11-deoxycortisol (precursor to cortisol) and cortisol
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