16 results
diagnosis pocus clinical peds signs a4c aortic genetics management plax 21hydroxylasedeficiency 21ohd alzheimersdisease anomalous aorta artery cardiac cardiogenic chondrocalcinosis collapse
D-Sign on Ultrasound Right Ventricular Pressure vs Volume Overload Eccentricity Index (EI) = D2/D1 RV Overload “D Sign” EI
D-Sign on Ultrasound ... RV Overload “D Sign ... @Pocus101 #DSign ... #Ultrasound #echocardiogram ... psax #diagnosis #cardiology
Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
Cardiogenic #Shock #pathophysiology ... #cardiology #diagnosis ... #signs #symptoms
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
#Fallot #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
The RAC sign = retroaortic coronary artery Dr. Kazi Ferdous @fazalabul #RAC #sign #retroaortic #coronary #artery #clinical
The RAC sign = retroaortic ... fazalabul #RAC #sign ... artery #clinical #ultrasound ... #cardiology #POCUS ... #echocardiogram
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 Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... Classic “snowman sign ... diagnosis #management #cardiology ... #peds #pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
chromosome 21) Signs ... / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
McConnell's Sign on POCUS Echocardiogram (A4C) A4c view; RV enlargement & hypokinesis with apical sparing ("McConnell Sign"
McConnell's Sign ... on POCUS Echocardiogram ... #POCUS #Echocardiogram ... A4C #clinical #ultrasound ... #cardiology
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