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diagnosis pediatrics endocrinology iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd cah causes comparison congenitaladrenalhyperplasia differential encephalopathy laboratory management metabolicemergency
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
Pediatrics in Review ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... #Neonatology #Peds
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Pediatrics In Review ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Table #NICU #Genetics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... #CAH #algorithm ... comparison #treatment #Peds ... Endocrinology #Adrenal ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Syndrome (PRES) Overview ... Immunosuppressive agents, Renal ... Etiology: • Pathophysiology ... Seizures: Treat with AEDs
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