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diagnosis pediatrics management neonatology nicu differential evaluation iem inbornerrors metabolism table 21hydroxylasedeficiency 21ohd admission antenatal classification counseling decisionaid diabetes diabetic
Differential Diagnosis for Failure to Thrive #Diagnosis #EM #Peds #PrimaryCare #FailureToThrive #FTT #Failure #Thrive #Differential #Algorithm
Thrive #Diagnosis #EM ... #Peds #PrimaryCare ... #Differential #Algorithm ... #Ddxof
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the ... Diagnosis #Management #EM ... #Peds #Trauma # ... HeadCT #PECARN #Algorithm ... #Ddxof
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... #Neonatology #Peds
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Table #NICU #Genetics
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Types of Skull Fractures #Diagnosis #EM #ENT #NSG #Skull #Fracture #Classification #Complications #Algorithm #Ddxof
Fractures #Diagnosis #EM ... Classification #Complications ... #Algorithm #Ddxof
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Diagnosis #Management #EM ... #Peds #Fever #Workup ... Discharge #Admission #Algorithm ... #Ddxof
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 ... #genetics #endocrinology ... #peds #pediatrics
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