11 results
diagnosis pathophysiology signs tetralogy chest chestxray fallot genetics xray 21hydroxylasedeficiency 21ohd aorta coarctation coins comparison cor cortriatriatum dehydration elbow endocrinology
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
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
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.
#Chest #XRay #CXR ... #clinical #radiology ... #peds #pediatrics ... #cardiology #ToF
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 ... pathophysiology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... , mastoiditis, febrile ... pathophysiology #diagnosis #symptoms ... #signs #peds #pediatrics
Pediatric Elbow Injuries - Elbow Xrays Check the fat pads on the lateral projection: 1. A displaced anterior
Pediatric Elbow ... fat pad (sail sign ... Injuries #Xrays #Radiology ... #peds #Pediatrics ... #clinical
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
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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