19 results
algorithm treatment cardiology disease fever genetics pneumonia stepbystep summary 21hydroxylasedeficiency 21ohd acquired adult alkaptonuria anomalous antenatal antibiotics arteriosus blackurine bronchiolitis
Step by Step Algorithmic Approach to Pediatric Fever Age < 21 days old (or 28 days for
Algorithmic Approach to Pediatric ... Leukocytes in the urine ... #Peds #Diagnosis ... #Management #StepByStep ... #Algorithm #Infant
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... loss Reduced urine ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Peds #Pediatrics
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... Complications #Peds
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Total Anomalous Pulmonary ... Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... #peds #pediatrics
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
anomalies • Pathophysiology ... Pre-operative management ... Cardiomegaly, increased pulmonary ... Truncus #Arteriosus #diagnosis ... #peds #pediatrics
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... leukocytes in urine ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile
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 pulmonale ... Syndrome #genetics #pathophysiology ... #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 ... non-arousable, decr urine ... endocrinology #peds ... #pediatrics
Bronchiolitis Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
symptoms for 1 ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #diagnosis #management ... #peds #treatment
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