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diagnosis diabetes differential genetics gestational idm maternal mother neonatology newborn nicu obgyn obstetrics screening 21hydroxylasedeficiency 21ohd antenatal classification counseling decisionaid
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... Mother - complications ... - pathophysiology ... #Pediatrics #Neonatology ... #Peds #Newborn
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
algorithm #Infant ... #Pediatrics #Neonatology ... #Maternal #Complications ... #Peds #Newborn ... #PatientInfo #Management
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Neonates and Infant ... Syndrome Older Infants ... #Causes #Peds # ... Pediatrics
Infant UTI Algorithm (<8 weeks of age) Emergency Medicine Cases @EMCases #Infant #Pediatric #UTI #Algorithm #Diagnosis #Management #UrinaryTractInfection
Infant UTI Algorithm ... Emergency Medicine Cases ... #Pediatric #UTI ... #Management #UrinaryTractInfection ... #Peds
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Sturge-Weber Syndrome Neonates ... #Causes #Peds # ... Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... Poor suckling -> Neonatal ... Obesity -> Type 2 diabetes ... Syndrome #genetics #pathophysiology ... #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 ... #algorithm #DM2
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 ... endocrinology #peds ... #pediatrics
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