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diagnosis neurology 21hydroxylasedeficiency endocrinology evaluation falls genetics geriatrics pathophysiology pediatrics recurrent spinal spinalcord
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 ... Labia major & minor ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Spinal Cord Disorders ... - Differential ... and signs below ... Sarcoidosis, Behcet disease ... #algorithm
Evaluation of Recurrent Falls Core Concept: Maintaining an upright posture requires the integrated function of multiple systems. Disruption in
Recurrent Falls Core ... presyncope, exertional symptoms ... positive Romberg sign ... Examples: - Dementia ... Falls #Diagnosis #Differential
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