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21ohd algorithm diagnosis hypotonic newborn
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... #Differential # ... #Peds #Pediatrics
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