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diagnosis peds complications diabetic gestational idm management maternal mother neonatology newborn nicu obgyn obstetrics pharmacology treatment 21hydroxylasedeficiency 21ohd adrenal algorithm
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... complications - pathophysiology ... : UpToDate #Infant ... #Pediatrics #Neonatology ... OBGYN #Diagnosis #Pathophysiology
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes ... algorithm #Infant ... #Diabetic #Mother ... #Pediatrics #Neonatology ... OBGYN #Diagnosis #Pathophysiology
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
ADH (SIADH) - Comparison ... Table Diabetes ... Insipidus #SIADH #Comparison ... #Table #Pathophysiology ... Symptoms #Diagnosis #Endocrinology
Comparison of anti-diabetic or anti-hyperglycemic agents There are numerous anti-hyperglycemic agents available to manage Type 2 diabetes.
Comparison of anti-diabetic ... This chart summarizes ... pharmacotherapy #table ... #comparison #management ... #endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis #comparison ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Insulin Comparison Chart Insulin Types - Onset (hours) - Peak Glycemic Effect (hours) - Duration (hours) •
Insulin Comparison ... Chart Insulin ... 10 #Insulin #Comparison ... #Table #pharmacology ... #diabetes #endocrinology
Fecal Incontinence - Pathogenesis and Complications Continence mechanisms are impaired • Local neuronal damage • External and
mechanisms are intact ... Diabetes) • Altered ... #Incontinence #geriatrics ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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