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differential genetics pathophysiology 21hydroxylasedeficiency 21ohd acute adult cough cyanosis disease distress dyspnea endocrinology incomplete infancy infant neonatal newborn praderwilli respiratory
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary ... respiratory #distress #causes
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Algorithm CXR ... #Algorithm #Causes ... #Peds #Pediatrics ... #Pulmonary
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm No Fever, No Tachypnea - Normal Chest Auscultation
Causes of Acute ... Pediatric Cough ... Bronchitis - No URTI Symptoms ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Algorithm Present ... #Algorithm #Causes ... #Peds #Pediatrics ... #Pulmonary
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Pediatric Dyspnea ... Algorithm Stridor ... Ketoacidosis • Pulmonary ... #Algorithm #Causes ... #Peds #Pediatrics
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 pulmonale ... pathophysiology #peds ... #pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... Algorithm Congenital ... Neurologic Anomaly • Pulmonary ... #Algorithm #Causes ... #Peds #Pediatrics
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm Peripheral Only: • Poor Perfusion • Acrocyanosis Hemoglobinopathy:
Causes of Cyanosis ... Algorithm Peripheral ... Total Anomalous Pulmonary ... #Algorithm #Causes ... #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 ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
suspected incomplete Kawasaki ... if they have no clinical ... purposes of this algorithm ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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