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diagnosis infant 21hydroxylasedeficiency 21ohd antenatal counseling decisionaid diabetes diabetic differential endocrinology genetics gestational idm management maternal mother neonatology newborn nutritional
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... Diabetic #Mother #Pediatrics ... Neonatology #IDM #NICU ... #Maternal #Complications ... #Peds #Newborn
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... Ductus Arteriosis (PDA ... Enterocolitis (NEC) Neurologic ... Differential #Diagnosis #Causes ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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