2 results
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 ... #peds #pediatrics
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