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comparison signs background clinical ct doses fallot genetics imaging nuclear pathophysiology patientinfo radiation risks study table testing tetralogy 21hydroxylasedeficiency 21ohd
Summary of problems of Very Low Birthweight Infants #Premature #Low #Birthweight #Peds #Pediatrics #Problems #Signs #Symptoms #Presentation
Low Birthweight Infants ... #Birthweight #Peds ... #Pediatrics #Problems ... #Signs #Symptoms
Coins on Chest XRay - Trachea vs Esophagus Coins in the sagittal plane on X-ray are more
#Coins #ChestXRay ... Trachea #Esophagus #Peds ... #Pediatrics #CXR ... #Radiology #Comparison
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Infant #Dehydration ... #Peds #Pediatrics
Estimated Medical Radiation Doses for 5 Year-Old Child 3-view ankle 0.0015 mSv 1/14th CXRs 2-view chest 0.02 mSv 1 CXRs Anteroposterior and lateral
American Academy of Pediatrics ... #PatientInfo #Radiology ... Doses #Imaging #ChestXRay ... Testing #Study #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
Tetralogy of Fallot - Chest XRay An 18-month-old male presents with his parents who have noticed that
Tetralogy #Fallot #ChestXRay ... #Clinical #Radiology ... #CXR #Peds #Pediatrics
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
How much radiation is used in paediatric radiology examinations compared to other exposures? Estimated dose - Days
radiation is used in paediatric ... Doses #Imaging #ChestXRay ... #CXR #CT #Nuclear ... Testing #Study #Peds ... #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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