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pediatrics 21hydroxylasedeficiency diagnosis differential endocrinology floppy genetics hypotonic pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Hypoglycemia • Early ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Diagnosis Algorithm ... • Hypoxic-Ischemic ... #Causes #Peds #
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