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diagnosis pediatrics management differential aliem causes em neonatology nicu treatment adrenal headct headtrauma iem inbornerrors metabolism pecarn table workup 21hydroxylasedeficiency
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
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
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds
PATIENT AGE >2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
Diagnosis #Management #Peds ... #EM #Algorithm ... HeadCT #PECARN #ALiEM
Adrenal Insufficiency - Differential Diagnosis Workup Algorithm Primary Adrenal Insufficiency: • Autoimmune primary adrenal insufficiency • Adrenoleukodystrophy,
Diagnosis Workup Algorithm ... Adrenoleukodystrophy, genetic ... Diagnosis #Workup #Algorithm ... #endocrinology
PATIENT AGE <2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
Diagnosis #Management #Peds ... #EM #Algorithm ... HeadCT #PECARN #ALiEM
Steroid Synthesis Pathway Dr. Caoimhe Costigan @CaoimheCostigan #Steroid #Synthesis #pathophysiology #algorithm #endocrinology
Steroid #Synthesis #pathophysiology ... #algorithm #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
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