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endocrinology 21hydroxylasedeficiency 21ohd adrenal algorithm cah children congenitaladrenalhyperplasia coronavirus covid19 examination hematology hemeonc hemophagocytic hlh infant inflammatory kawasaki lymphohistiocytosis management
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... #diagnosis #comparison ... #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Multi-System Inflammatory Syndrome in Children (MIS-C) vs. Kawasaki Disease CDC Case Definition for MIS-C; • < 21
Kawasaki Disease CDC ... Case Definition ... MISC #Kawasaki #Comparison ... #diagnosis #peds ... #pediatrics #COVID19
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... When the diagnosis ... paediatrician or geneticist ... #Examination #Peds ... #Pediatrics #Diagnosis
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... Familial) HLH: - Genetic ... Presentation • Common Signs ... Pathophysiology ... of NK cells and CD8
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