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pathophysiology 21hydroxylasedeficiency crypto cryptococcal diabetes diabeticketoacidosis dka genetics mri pediatrics peds radiology t2
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Pathogenesis and Clinical ... out of cells may cause ... renal function/urine ... be used by the brain ... Signs/Symptoms/Complications
Cryptococcal meningitis on T2 MRI 30 M from sub-Saharan Africa presents w/ progressive Headache x1 mo, +neck
organism (soap bubble sign ... Nausea & vomiting ... of K+ & Mg in urine ... #T2 #MRI #Brain ... #clinical #radiology
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