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21hydroxylasedeficiency 21ohd als diagnosis endocrinology genetics lateral management neurology sclerosis
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
Amyotrophic Lateral ... combination of the clinical ... lateral sclerosis Pathophysiology ... features developing later ... conditions listed in differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... , vomiting • Late ... endocrinology #peds ... #pediatrics
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