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diagnosis peds complications congenital diabetic endocrinology genetics gestational idm infections maternal mother neonatology newborn nicu obgyn obstetrics torch 21hydroxylasedeficiency 21ohd
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 ... #Signs #Symptoms
Congenital TORCH Infections Dr. Natalie Marshall @MicrobeNat #Congenital #Infections #Comparison #Table #pediatrics #diagnosis #symptoms #TORCH
Congenital #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
Congenital Infections - Comparison Table: Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus Manifestations: Anemia, Bony
Congenital Infections - Comparison ... Table: Infections ... Congenital #Infections #Comparison ... #Table #pediatrics ... #diagnosis #symptoms
Fecal Incontinence - Pathogenesis and Complications Continence mechanisms are impaired • Local neuronal damage • External and
mechanisms are intact ... Diabetes) • Altered ... #Incontinence #geriatrics ... #pathophysiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... Obesity -> Type 2 diabetes ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
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