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21hydroxylasedeficiency brain clinical crypto cryptococcal diagnosis differential encephalitis genetics infections mri neurology pathophysiology pediatrics peds radiology t2
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 ... pathophysiology #genetics #endocrinology
CNS Infections - Viral Encephalitis and Bacterial Meningitis - Differential Diagnosis Framework Viral Encephalitis: MCC: Enteroviruses (e.g., coxsackievirus
CNS Infections - ... Photophobia • Nausea ... Acute meningeal signs ... established by CSF or urine ... Singh @rav7ks #CNS
Cryptococcal meningitis on T2 MRI 30 M from sub-Saharan Africa presents w/ progressive Headache x1 mo, +neck
Cryptococcal meningitis ... low glucose) CNS ... organism (soap bubble sign ... Nausea & vomiting ... of K+ & Mg in urine
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