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diagnosis acutepe genetics pathophysiology 21hydroxylasedeficiency 21ohd adult algorithm anomalous causes clinical criticalcare cxr differential distress dsign echocardiogram emergencymedicine fallot hamptonhump
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... differential #neonatal #pediatrics ... #adult #peds #pulmonary
Pulmonary Embolism - Signs and Symptoms Most Common Presenting SYMPTOMS - Dyspnea at rest or with
Pulmonary Embolism ... - Signs and Symptoms ... Common Presenting SIGNS ... distension (14%) #PulmonaryEmbolism ... #AcutePE #Signs
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Diagnostic Algorithm for Suspected Pulmonary Embolism Well's Criteria for PE • Clinical Signs and Symptoms of DVT
for Suspected Pulmonary ... Embolism Well's ... PE • Clinical Signs ... and Symptoms of ... months) - 1.0 #PulmonaryEmbolism
D-Sign in Pulmonary Embolism on POCUS Echocardiogram - PSAX Pt having shortness of breath? POCUS can shed
D-Sign in Pulmonary ... Embolism on POCUS ... D-sign = high RV ... PSAX #clinical #cardiology ... #PulmonaryEmbolism
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 Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classic “snowman sign ... Total #Anomalous #Pulmonary ... diagnosis #management #cardiology ... #peds #pediatrics
Hampton hump is a radiologic sign which consists of a shallow wedge-shaped opacity in the periphery
is a radiologic sign ... embolism. ... In this case, pulmonary ... embolism was confirmed ... #PE #PulmonaryEmbolism
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... sleep apnea, cor pulmonale ... pathophysiology #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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