17 results
radiology diagnosis management nejm chestxray genetics mri obstetrics pregnancy sign tetralogy xray 21hydroxylasedeficiency 21ohd adrenal aflp anatomy aortic aorticvalve axr
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... > Neonatal and infantile ... , sleep apnea, cor ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Coins on Chest XRay - Trachea vs Esophagus Coins in the sagittal plane on X-ray are more
Trachea #Esophagus #Peds ... #Pediatrics #CXR ... #Radiology #Comparison ... #Clinical
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Introduction & Pathophysiology ... Epidemiology • Clinical ... #AorticValve #cardiology ... #peds #pediatrics
Cor triatriatum • Epidemiology • Etiology • Associated Lesions • Differentials Diagnosis • Anatomy - Sinister,
Cor triatriatum ... Physiology • Clinical ... diagnosis #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 ... #Chest #XRay #CXR ... #clinical #radiology ... #peds #pediatrics ... #cardiology #ToF
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... = nonspecific (nausea ... AP, ↑INR, ↑BUN/Cr ... Maternal Support - Critical ... diagnosis #management #pathophysiology
Plain radiography of the abdomen revealed calcification of both adrenal glands. A homozygous mutation in LIPA
acid lipase is critical ... accumulation in the liver ... and gut, which causes ... #clincial #peds ... NEJM #Wolmans #radiology
Tetralogy of Fallot - Chest XRay An 18-month-old male presents with his parents who have noticed that
Fallot #ChestXRay #Clinical ... #Radiology #CXR ... #Peds #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... Sign #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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 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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
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