33 results
diagnosis management comparison pediatrics treatment neurology syndrome algorithm cardiology endocrinology iem inbornerrors metabolism neonatology nicu ophthalmology workup 21hydroxylasedeficiency 21ohd aafp
Causes, Symptoms, and Signs of Vaginitis #Vaginitis #Differential #Diagnosis #Comparison #Table #Gynecology #OBGyn #BV #Differential #Signs
Causes, Symptoms ... , and Signs of Vaginitis ... #Vaginitis #Differential ... Diagnosis #Comparison #Table ... #Signs #AAFP
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 A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table ... #NICU #Genetics
Typical Clinical Features of Major Causes of Acute Chest Discomfort #ChestPain #Features #Signs #Symptoms #Comparison #Table #Characteristics
Typical Clinical ... Features of Major Causes ... ChestPain #Features #Signs ... #Symptoms #Comparison ... #Table #Characteristics
Etiologies of Hypoaldosteronism Hyporeninemic Hypoaldosteronism (Low Renin, Low Aldosterone) - Diabetic Nephropathy - NSAIDs Non-Hyporeninemic Hypoaldosteronism (Normal
insufficiency - Critical ... illness - Genetic ... Hypoaldosteronism #Differential ... Aldosterone #Comparison #Table ... #Causes
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... #pathophysiology ... #peds #pediatrics
Summary of clinical findings for patients with encephalitis, by cause #Encephalitis #Signs #Symptoms #Table #Diagnosis #Differential #CSF
Summary of clinical ... encephalitis, by cause ... #Encephalitis #Signs ... #Symptoms #Table ... #Diagnosis #Differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #genetics #endocrinology ... #peds #pediatrics
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
with previously stable ... hypertension and signs ... 109 mm Hg) with clinical ... renal bruit or signs ... #Differential #
Chronic Hypertensive Retinopathy: Pathogenesis and clinical findings Ophthalmic Artery Hypertension Stage 1: Mild/vasoconstrictive • Acute and chronic vasospasm
Pathogenesis and clinical ... Hypertension Stage ... #Retinopathy #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms #complications
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