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diagnosis differential constipation infant physicalexam 21hydroxylasedeficiency 21ohd brudzinskis clinical dehydration disease dyspnea endocrinology floppy genetics hypotonic incomplete kawasaki meningitis newborn
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Differential Diagnosis Algorithm ... Hemangioma • Vocal Cord ... #Causes #Peds # ... Pediatrics #Pulmonary
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Disease • Spinal Cord ... #Causes #Peds # ... Pediatrics
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Pediatric Dyspnea ... Differential Diagnosis Algorithm ... Foreign Body Decreased ... #Causes #Peds # ... Pediatrics
Pediatric Constipation - Differential Diagnosis Algorithm Dietary/Functional • lnsufficient Volume / Bulk Neurologic • Hirschsprung's Disease • Imperforate
Pediatric Constipation ... Differential Diagnosis Algorithm ... Disease • Spinal Cord ... #Constipation #Pediatric ... #Causes #Peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds # ... Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
in an infant Decreased ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... spinal cord movement ... #PhysicalExam #Pediatrics ... #Peds
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... Late (shock): cold ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
purposes of this algorithm ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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