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peds screening 21hydroxylasedeficiency antenatal classification complications counseling decisionaid diabetic diagnosis dm2 dmii genetics gestational idm maternal mother neonatology newborn nicu
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes ... algorithm #Infant ... #Pediatrics #Neonatology ... OBGYN #Diagnosis #Pathophysiology ... #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 ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Type 2 Diabetes - Screening, Diagnosis and Management Algorithm Lifestyle Modifications (Diet and Exercise) -> Start
Diagnosis and Management ... Algorithm Lifestyle ... OR macrosomic infant ... • Secondary Causes ... Endocrinopathies (Cushing Syndrome
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