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21hydroxylasedeficiency diagnosis differential encephalitis genetics infections pathophysiology peds
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 ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD ... #peds #pediatrics
CNS Infections - Viral Encephalitis and Bacterial Meningitis - Differential Diagnosis Framework Viral Encephalitis: MCC: Enteroviruses (e.g., coxsackievirus
CNS Infections - ... Acute meningeal signs ... established by CSF or urine ... Singh @rav7ks #CNS ... differential #diagnosis #neurology
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