104 results
Hyperglycemia - Differential Diagnosis Algorithm
Diabetes Mellitus:
 • Impaired Glucose Tolerance
 • Type I Diabetes
 • Type
Hyperglycemia - ... agonists • Others Critical ... Stress: • Stress Hyperglycemia ... Infarction #Hyperglycemia ... Diagnosis #Algorithm #endocrinology
Adrenal Insufficiency Differential Diagnosis Algorithm
Clinical suspicion: Weakness, fatigue, nausea, musculoskeletal pain, dizziness, volume depletion, abdominal pain,
Diagnosis Algorithm Clinical ... hyperpigmentation, hypoglycemia ... Diagnosis #Algorithm #endocrinology
Hypoglycemia - Differential Diagnosis Algorithm
Fasting Hypoglycemia:
 • Excess Insulin
 • Medications (e.g. Insulin Secretagogues, ß-Adrenergic Antagonists,
Hypoglycemia - Differential ... Algorithm Fasting Hypoglycemia ... Other Causes: • Critical ... Anorexia Nervosa #Hypoglycemia ... Diagnosis #Algorithm #endocrinology
Regression of Clubbing after Treatment of Lung Cancer #Clinical #PhysicalExam #Radiology #Clubbing #Regression #LungCancer #CT #NEJM
of Lung Cancer #Clinical ... #PhysicalExam #Radiology ... LungCancer #CT #NEJM
Hyperkalemia after Missed Hemodialysis - Initial electrocardiogram showed peaked T waves and a prolonged QT segment
segment (Panel A) #Clinical ... #Cardiology #EM ... Hyperkalemia #PeakedT #NEJM
Adrenal Insufficiency Diagnosis Algorithm
Clinical features: 
 - Weight loss, anorexia, Weakness, fatigue, GI distress
 - Hypotension,
Diagnosis Algorithm Clinical ... - Unexplained hypoglycemia ... Stimulation #StimTest #Endocrinology
Nystagmus from Wernicke’s Encephalopathy - Magnetic resonance imaging of the brain showed T2 hyperintensities involving the
#Clinical #Radiology ... MRI #Thalamus #NEJM
GIANT Left Main Coronary Artery Aneurysm

49-year-old man with hypertension was referred for evaluation of recurrent angina.
Artery #Aneurysm #Clinical ... #Fluoroscopy #Cardiology ... #NEJM
Creutzfeldt-Jakob Disease - Magnetic resonance imaging (MRI) revealed hyperintensity of the cortical gyri of the frontal
#Clinical #Neuro ... #Radiology #MRI ... CreutzfeldJakob #NEJM
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Hyperkalemia, Hypoglycemia ... pathophysiology #genetics #endocrinology