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21hydroxylasedeficiency diagnosis differential endocrinology evaluation falls genetics geriatrics neurology pathophysiology peds recurrent
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... • This is also ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Evaluation of Recurrent Falls Core Concept: Maintaining an upright posture requires the integrated function of multiple systems. Disruption in
the integrated function ... ) - Spinal cord ... neuron disease (ALS ... weakness, muscle wasting ... fear of falling, functional
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