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diagnosis inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd agammaglobulinemia algorithm anatomy circulation differential endocrinology fallot fetal immunology laboratory management metabolicemergency
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Neonatology #Peds ... #IEM #NICU #InbornErrors
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
See IEM schema for ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #NICU #Genetics ... #IEM #Laboratory
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... diagnosis #management #cardiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
X-Linked Agammaglobulinemia: Pathogenesis and clinical findings The epidemiology of this disease is 1/340,000 births and roughly double
immunodeficiency may appear 3-9 ... Genetic Predisposition ... to produce all classes ... IgA, IgG, and IgM ... Agammaglobulinemia #XLinked #pathophysiology
Fetal and Post Transition Circulation In the fetal circulatory system, oxygenated blood is delivered via the umbilical
oxygenated blood passes ... #Circulation #Pathophysiology ... #Cardiology #Anatomy ... #Peds #Pediatrics
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