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diagnosis differential neurology 21hydroxylasedeficiency endocrinology genetics management myelitis pediatrics spinal spinalcord transverse
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Spinal Cord Disorders ... • Symptoms and signs ... Cauda equina- decreased ... #spinalcord #disorders ... differential #algorithm
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
Focal inflammatory disorder ... monophasic Pathophysiology ... - Reflexes: decreased ... • Bilateral signs ... , MOG antibody disorders
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