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peds obstetrics diabetes diabetic differential endocrinology gestational idm management maternal mother neonatology newborn nicu 21hydroxylasedeficiency 21ohd adrenal aflp algorithm alzheimersdisease
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... - pathophysiology ... Diabetic #Mother #Pediatrics ... Neonatology #IDM #NICU #OBGYN ... #Diagnosis #Pathophysiology
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... Neonatology #IDM #NICU #OBGYN ... #Diagnosis #Pathophysiology ... #Maternal #Complications
Comparison of Causes of Salt-Wasting in Infancy - PHA 1 - PHA 3 - 21-OH CAH
Comparison of Causes ... Salt-Wasting in Infancy ... #Comparison #Causes ... #differential #diagnosis ... #pediatrics #nephrology
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... - Differential Diagnosis ... #Complications ... #Causes #Peds # ... Pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... #diagnosis #comparison ... Endocrinology #Adrenal #pathophysiology
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... = nonspecific (nausea ... , ↑Tbili/Dbili/AP ... Monitor and Treat Complications ... hepatology #obstetrics #obgyn
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Alzheimer's (99% of cases ... Alzheimer's (1% of cases ... Signs / Symptoms / Complications ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
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 #pediatrics
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