35 results
diagnosis treatment neurology algorithm differential signs symptoms gastroenterology pediatrics peds rheumatology barre comparison diabetes diabetic genetics guillain gynecology hematology ketoacidosis
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table Diabetes Insipidus - Inadequate ADH SIADH -
Diabetes Insipidus vs Syndrome ... Comparison #Table #Pathophysiology ... Symptoms #Diagnosis #Endocrinology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... delayed puberty -> Infertility ... #PraderWilli #Syndrome ... #genetics #pathophysiology
Wolfram syndrome (WS) is a form of monogenic diabetes that typically presents with diabetes mellitus in
Wolfram syndrome ... hypogonadism, infertility ... WOLFRAMSYNDROME #SUMMARY #ENDOCRINOLOGY
Pathophysiology of Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar Syndrome (HHS) Absolute Insulin deficit: - Type I DM:
Pathophysiology ... Hyperglycemic Hyperosmolar Syndrome ... #dka #hhs #pathophysiology ... #comparison #endocrinology
Irritable Bowel Syndrome (IBS) - Pathophysiology, Diagnosis and Management Algorithm Risk factors: Previous acute enteric infection, Female
Irritable Bowel Syndrome ... (IBS) - Pathophysiology ... Diagnosis and Management ... #Pathophysiology ... #Diagnosis #Management
Management of Polycystic Ovary Syndrome (PCOS) Hyperandrogenism, Family Planning, Endometrial cancer prevention, Cardiovascular risk factor management → Weight
Management of Polycystic ... Ovary Syndrome ... Cardiovascular risk factor management ... Polycystic #Ovary #Syndrome ... #Management #endocrinology
Hypocalcemia - Diagnosis and Management PTH Independent (↑ PTH) • LOW VIT D -
Diagnosis and Management ... Formation: Hungy Bone Syndrome ... - DiGeorge Syndrome ... Hypocalcemia #Diagnosis #Management ... #endocrinology
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... Associated Genetic Syndromes ... palliation • Post-Op Management ... Fallot #diagnosis #management
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Management of Necrotizing Pancreatitis Severe Pancreatitis Pathophysiology Diagnosis of Pancreatic Necrosis Infected Necrosis Complications of Severe Pancreatitis: 1) Pancreatic Fistula 2) Disconnected
Management of Necrotizing ... Pancreatitis Pathophysiology ... Pancreatic Duct Syndrome ... #Pancreatitis #Management
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