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pediatrics peds 21hydroxylasedeficiency antenatal counseling decisionaid diabetes diabetic diagnosis endocrinology genetics gestational idm maternal mother neonatology newborn nicu nutritional obgyn
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications ... #PatientInfo #Management
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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
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