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diagnosis management comparison treatment algorithm endocrinology iem inbornerrors metabolism neonatology nicu signs syndrome 21hydroxylasedeficiency 21ohd abscess acromegaly age aldosterone alopecia
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table ... #NICU #Genetics
Common pediatric rashes you see in clinic. How to differentiate them? Name that rash. #pediatrics #peds #rashes
Common pediatric ... How to differentiate ... #pediatrics #peds ... #rashes #clinical ... #comparison #table
Web chart of etiologies related to inflammatory head and neck masses. #pediatrics #peds #differential #causes #pearls #head
#pediatrics #peds ... #differential # ... causes #pearls # ... head #neck #masses ... viral #bacterial #clinical
Causes of Developmental Delay - Differential Diagnosis Algorithm Isolated Domain Delay - Reduced Respiratory Drive: • Cognitive
Causes of Developmental ... Delay - Differential ... Syndromic • Genetic ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Epiglottitis - Swollen inflamed epiglottis Clinical (Rapid onset) • Fever • Sore throat
inflamed epiglottis Clinical ... Epiglottitis #Signs #Causes ... #Diagnosis #Differential ... #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Etiologies of Hypoaldosteronism Hyporeninemic Hypoaldosteronism (Low Renin, Low Aldosterone) - Diabetic Nephropathy - NSAIDs Non-Hyporeninemic Hypoaldosteronism (Normal
insufficiency - Critical ... illness - Genetic ... Hypoaldosteronism #Differential ... Aldosterone #Comparison #Table ... #Causes
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... Tachypnea #Wheeze #Differential
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