5 results
diagnosis management 21hydroxylasedeficiency 21ohd adrenal algorithm cah cardiology causes comparison congenitaladrenalhyperplasia fallot hematology hemeonc hemophagocytic hlh immunization lymphohistiocytosis tetralogy
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds ... #pediatrics #treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
Childhood Immunization ... & seizures are late ... bacteremia are late ... #Immunization #peds ... #pediatrics #pathophysiology
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
the trigger is difficult ... Familial) HLH: - Genetic ... infancy or early childhood ... Pathophysiology ... Treatment Approach
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