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diagnosis differential genetics endocrinology iem inbornerrors metabolism neonatology nicu treatment 21hydroxylasedeficiency 21ohd adrenal brudzinskis cah chloride clinical comparison congenitaladrenalhyperplasia disease
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #Pediatrics #Table
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Pediatric Dyspnea - Differential Diagnosis Algorithm Stridor: • Croup • Foreign Body • Tracheitis • Epiglottitis •
Pediatric Dyspnea ... Differential Diagnosis Algorithm ... Foreign Body Decreased ... #Causes #Peds # ... Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... AP Stable? ... Signs of shock or ... #peds #Pediatric
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... Differential #Diagnosis #Algorithm ... #Pathophysiology
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 ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
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 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
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... 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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