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peds 21hydroxylasedeficiency 21ohd complications diagnosis differential genetics premature preterm
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Respiratory Distress Syndrome ... Enterocolitis (NEC ... ) Neurologic: ... Differential #Diagnosis #Causes ... #Peds #Pediatrics
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