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diagnosis management 21hydroxylasedeficiency encephalopathy endocrinology fungal genetics infections infectiousdiseases mycoses pediatrics peds posterior pres reversible syndrome
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
may precede the neurologic ... Etiology: • Pathophysiology ... Neurological symptoms ... sequences improve sensitivity ... Seizures: Treat with AEDs
Mycoses HISTOPLASMOSIS • Inhalation of conidia → Yeast → travel to lymph nodes → spread in body • Bird
antigen assay has a sensitivity ... has five major clinical ... fungal stain of clinical ... yeast • At risk: AIDS ... Aspergillosis Pathophysiology
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