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diagnosis pediatrics obstetrics diabetes diabetic gestational idm infant management maternal mother neonatology newborn nicu pregnancy 21hydroxylasedeficiency 21ohd adrenal aflp antenatal
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Diabetic Mother - complications ... - pathophysiology ... learning schema ... Neonatology #IDM #NICU #OBGYN ... #Peds #Newborn
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... Neonatology #IDM #NICU #OBGYN ... #Diagnosis #Pathophysiology ... #Maternal #Complications ... #Peds #Newborn
Causes of Growth Discrepancy: Large for Gestational Age - Differential Diagnosis Algorithm Maternal Factors: • Multiparity •
Causes of Growth ... Differential Diagnosis Algorithm ... Excessive weight gain ... #Causes #Obstetrics ... #OBGyn
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... = nonspecific (nausea ... vomiting, abdominal pain ... Monitor and Treat Complications ... hepatology #obstetrics #obgyn
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
URT inflammation causes ... leading to organ ischemia ... jaundice and RUQ pain ... #Immunization #peds ... #pediatrics #pathophysiology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
out of cells may cause ... Signs/Symptoms/Complications ... • Abdominal pain ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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