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diagnosis obgyn pediatrics diabetes genetics gestational idm liver management maternal mother neonatology newborn nicu pregnancy 21hydroxylasedeficiency 21ohd aflp algorithm antenatal
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... Mother - complications ... - pathophysiology ... #Peds #Newborn ... #Obstetrics #Diabetes
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
algorithm #Infant ... OBGYN #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn ... #Obstetrics #Diabetes
Causes of Growth Discrepancy: Large for Gestational Age - Differential Diagnosis Algorithm Maternal Factors: • Multiparity •
co-morbidities (e.g. diabetes ... lbs) Maternal Complications ... Factors: • Male infant ... syndrome) Fetal Complications ... Algorithm #Causes #Obstetrics
Fecal Incontinence - Pathogenesis and Complications Continence mechanisms are impaired • Local neuronal damage • External and
Pathogenesis and Complications ... mechanisms are intact ... Diabetes) • Altered ... Incontinence #geriatrics #pathophysiology
The Liver Consult Primer - Guide to calling a consult HPI: - Start with reason for consult
- Cirrhosis & complications ... liver biopsy Meds ... - Outpatient meds ... Calling #Referral #Hepatology ... #Gastroenterology
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... Monitor and Treat Complications ... Liver #Pregnancy #hepatology ... #obstetrics #obgyn ... diagnosis #management #pathophysiology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Signs/Symptoms/Complications ... 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
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