15 results
diagnosis dka ketoacidosis syndrome genetics gestational idm infant maternal mother neonatology newborn nicu obgyn obstetrics signs 21hydroxylasedeficiency 21ohd antenatal bulimianervosa
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... UpToDate #Infant #Diabetic ... #Mother #Pediatrics ... #Peds #Newborn ... #Obstetrics #Diabetes
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes ... algorithm #Infant #Diabetic ... #Mother #Pediatrics ... #Obstetrics #Diabetes ... #Gestational #Diabetes
Diabetic Ketoacidosis Management Priorities 1. Fluids 2. Insulin 3. Potassium 4. Acidosis 5. Re-establish oral fluids,
Diabetic Ketoacidosis ... #DKA #Diabetic ... #Ketoacidosis #Diabetes ... #Management #Pediatrics ... #Peds
Diabetic Ketoacidosis (DKA) - Diagnosis and Management Summary Symptoms: • Abdominal pain • Nausea • Polyuria • Polydipsia • Vomiting • Weight loss •
Diabetic Ketoacidosis ... Summary Symptoms ... Abdominal pain • Nausea ... mg/dL #DKA #Diabetic ... #Endocrinology
Diabetic Ketoacidosis (DKA) - Diagnosis and Management Summary Symptoms: • Abdominal pain • Nausea • Polyuria • Polydipsia • Vomiting • Weight loss •
Diabetic Ketoacidosis ... Summary Symptoms ... Abdominal pain • Nausea ... mg/dL #DKA #Diabetic ... #Endocrinology
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... /Complications: ... Obesity -> Type 2 diabetes ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
Diabetic Ketoacidosis ... Signs/Symptoms/Complications ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology ... #diabetes
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
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
Signs / Symptoms ... / Complications ... Hyperprolactinemia • Diabetes ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
Refeeding Syndrome Overview What Is It? • Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
changes and may cause ... severe clinical complications ... Poorly controlled diabetes ... overload) Other Symptoms ... Differential #Diagnosis #Pathophysiology
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