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diagnosis endocrinology management 21hydroxylasedeficiency 21ohd acromegaly brudzinskis encephalopathy genetics meningitis neurology posterior pres reversible sign treatment video
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 ... non-arousable, decr urine ... endocrinology #peds ... #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... Sign #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
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 Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Etiology: • Pathophysiology ... Drug toxicity, Metabolic ... the underlying cause ... Seizures: Treat with AEDs ... until cause identified
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
GrepMed Handbook Clinical ... Hypogonad (50%) • Metabolic ... Beckwith Wiedemann syndrome ... Diagnosis and Workup ... or refractory cases
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