10 results
diagnosis pathophysiology radiology chestxray genetics management tetralogy 21hydroxylasedeficiency 21ohd ascorbicacid chest coins comparison cor cortriatriatum dehydration endocrinology esophagus fallot falot
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
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Pale or Mottled Skin ... PhysicalExam #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
integrity of: • Skin ... poor nutrition Clinical ... Psychiatric symptoms ... : • Petechia • ... • Petechiae, purpura
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 1) Suggestive clinical manifestations
Henoch-Schönlein Purpura ... 1) Suggestive clinical ... individuals - Clinical ... #Rheumatology #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
Pathogenesis and clinical ... Syndrome Signs/Symptoms ... , sleep apnea, cor ... pathophysiology #peds ... #pediatrics
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 ... Signs/Symptoms/Complications ... cold & mottled skin ... endocrinology #peds ... #pediatrics
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings Parasomnias - Micro-arousal episodes during SWS -> Intense activation of
Pediatric Parasomnias ... Pathogenesis and clinical ... Speech • Flushed skin ... #Peds #pathophysiology ... #symptoms #pharmacology
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