16 results
diagnosis pediatrics management genetics signs comparison endocrinology iem inbornerrors metabolism neonatology nicu pharmacology syndrome 21hydroxylasedeficiency 21ohd algorithm aortoenteric assessment childhood
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
some diagnostic clues ... Assessment #Signs #Symptoms ... PhysicalExam #Diagnosis #Peds
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... connections and pathophysiology ... the lab values table ... #Neonatology #Peds ... #Pediatrics #Table
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... #Pathophysiology ... #Signs #Symptoms
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
Types of Chronic Urinary Incontinence Type, Prevalence, Pathophysiology and Symptoms: - Stress - Urge - Mixed -
Type, Prevalence, Pathophysiology ... and Symptoms: ... Types #Comparison #Table
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
TRALI vs TACO - Transfusion Reactions TRALI: • Epidemiology: 0.1% of transfused patientsl • Risk factors: Critical
blood donor • Pathophysiology ... ARDS to explain symptoms ... transfusion • Pathophysiology ... diagnosis #comparison #table
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Glaucoma - Emergency Department Management - All patients should get emergency ophthalmologic consultation - Start with eye drops
eye drops (see table ... or refractory symptoms ... blocker) - Topical meds ... #Medications #Table
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