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diagnosis treatment antiarrhythmics cardiology classes comparison differential management pediatrics peds pharmacology 21hydroxylasedeficiency 21ohd acidosis acromegaly adrenal cah clinicopathology congenitaladrenalhyperplasia diabetes
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Lymphomas and Lymphoproliferative Disorders - Differential Diagnosis Algorithm Hodgkin Lymphoma ~40% - Characteristic For Reed-Sternberg (RS) Cells
Differential Diagnosis Algorithm ... spread, B symptoms not ... Lymphoproliferative #Disorders #Classification ... #pathophysiology ... #differential #algorithm
Lactic Acidosis - Overview and Pathophysiology Lactic acid is an endogenous substrate for gluconeogenesis, that is constantly
- Overview and Pathophysiology ... is why LR does not ... cause acidosis) ... differential #diagnosis #pathophysiology ... #classification
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Clinical Findings • Note ... out of cells may cause ... Abdominal pain, nausea ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
Hashitoxicosis ‘Leakage’ symptoms of active Hashimoto’s disease - Hashitoxicosis (Htx) can occur during the initial hyperthyroid stage in
thyroiditis that causes ... hyperthyroidism) before not ... Hashitoxicosis #Hashimotos #Endocrinology ... #Diagnosis #Pathophysiology
Antiarrhythmics - Vaughan Williams Classification: CLASS 1 - Sodium Channel Blockers: • MOA: Block fast Na+ channels
Vaughan Williams Classification ... to prolong AV node ... to prolong AV node ... #Pharmacology #Classification ... #Classes #pathophysiology
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
For pituitary masses ... Typically (but not ... Headaches • Nausea ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... hyperkalemia do not ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Vaughan Williams Classification ... to prolong AV node ... to prolong AV node ... #Pharmacology #Classification ... #Classes #pathophysiology
Management of Hyponatremia Hypertonic Saline - Only indicated if patient has severe symptoms + Na < 125 Give
of Tolvaptan if not ... FEUrate > 11% • If not ... SIADH — look for cause ... hourly • Identify Cause ... Hyponatremia #Management #algorithm
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