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diagnosis pediatrics differential obstetrics diabetes diabetic gestational idm maternal mother neonatology nicu 21hydroxylasedeficiency 21ohd antenatal counseling decisionaid endocrinology epilepsy floppy
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... - pathophysiology ... learning schema ... Neonatology #IDM #NICU #OBGYN ... #Peds #Newborn
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn
Causes of Pediatric Spells - Differential Diagnosis Algorithm Neonates and Infant Spells: • Benign Sleep Myoclonus •
Causes of Pediatric ... Neonates and Infant ... Syndrome Older Infants ... • Transient Ischemic ... #Causes #Peds #
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... • Transient Ischemic ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Causes of Growth Discrepancy: Large for Gestational Age - Differential Diagnosis Algorithm Maternal Factors: • Multiparity •
Causes of Growth ... Differential Diagnosis Algorithm ... Factors: • Male infant ... #Causes #Obstetrics ... #OBGyn
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... Tachypnea of the Newborn ... #Complications ... Differential #Diagnosis #Causes ... #Peds #Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Diagnosis Algorithm ... • Hypoxic-Ischemic ... #Causes #Peds #
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 ... endocrinology #peds
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