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diagnosis management diabetes ketoacidosis pediatrics diabetic 21hydroxylasedeficiency 21ohd acromegaly adrenal algorithm anemia aplastic cah cardiology causes comparison congenitaladrenalhyperplasia fallot hematology
Pathophysiology and Effects of Insulin Deficiency #Insulin #Deficiency #DKA #Ketoacidosis #Diabetes #Pathophysiology #Endocrinology
Pathophysiology ... Effects of Insulin Deficiency ... #Insulin #Deficiency ... #DKA #Ketoacidosis ... #Endocrinology
Pathogenesis of Diabetic Ketoacidosis - Insulin deficiency or severe insulin insensitivity #DKA #Pathophysiology #Endocrinology #Diabetes #Ketoacidosis
Ketoacidosis - Insulin deficiency ... insensitivity #DKA ... #Pathophysiology ... #Endocrinology
Pathogenesis and Pathophysiology of Diabetic Ketoacidosis (DKA) DKA is a result of an absolute or relative insulin
Pathogenesis and Pathophysiology ... relative insulin deficiency ... details of the pathophysiology ... #Pathophysiology ... #Diabetes #Endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds ... #pediatrics #treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... amount of enzyme deficiency ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
Lymphohistiocytosis (HLH) Pathophysiology ... salmonella, ...), Parasites ... Cellular immune deficiency ... Unknown cause Treatment ... diagnosis #management #treatment
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Syndromes: - Genetic ... cells to repair DNA ... anemia, GATA2 deficiency ... , CTLA4 deficiency ... aplastic anemia Treatment
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
malignancy Pathophysiology ... phenytoin, minoxidil), genetic ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology
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