21 results
treatment summary syndrome differential genetics pathophysiology radiology signs 21hydroxylasedeficiency 21ohd adult algorithm anomalous aortic aorticvalve arteriosus bicuspid cardiomyopathy checkpointinhibitors chest
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary ... respiratory #distress #causes
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Syndrome Signs/Symptoms ... sleep apnea, cor pulmonale ... pathophysiology #peds ... #pediatrics
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... PVO Present • Diagnosis ... Return #TAPVR #diagnosis ... #management #cardiology ... #peds #pediatrics
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
Pre-operative management ... Cardiomegaly, increased pulmonary ... Truncus #Arteriosus #diagnosis ... #management #cardiology ... #peds #pediatrics
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Epidemiology • Clinical ... • Radiologic/Diagnostic ... Pre-operative Management ... #AorticValve #cardiology ... #peds #pediatrics
Cor triatriatum • Epidemiology • Etiology • Associated Lesions • Differentials Diagnosis • Anatomy - Sinister,
Physiology • Clinical ... Post-Operative Management ... #management #cardiology ... #summary #peds ... #pediatrics
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
boot shaped heart caused ... along with concave Pulmonary ... Chest #XRay #CXR #clinical ... #radiology #peds ... #pediatrics #cardiology
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 ... endocrinology #peds ... #pediatrics
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
and Management ... extrapulmonary cases ... Clinical Signs ... of active pulmonary ... for concomitant pulmonary
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
and Management ... renal failure Clinical ... Pulmonary: dyspnea ... acute sarcoidosis Pulmonary ... #Management #Signs
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