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21hydroxylasedeficiency amyotrophic diagnosis endocrinology genetics lateral management neurology pediatrics peds sclerosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... • This is also ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... disrupt cellular function ... multiple spinal cord ... - Further testing
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