9 results
diagnosis causes pediatrics diabetes differential ketoacidosis diabetic 21hydroxylasedeficiency 21ohd adrenal cah comparison congenitaladrenalhyperplasia diarrhea genetics hemophagocytic hlh hypophosphatemia insulin lowphosphate
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
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
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
Causes of Pediatric Diarrhea - Differential Diagnosis Algorithm Infectious: • Viral • Bacterial • Parasitic Malabsorption: • Lactase
Differential Diagnosis Algorithm ... Bacterial • Parasitic ... Primary Immuno-Deficiency ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Hypophosphatemia - Differential Diagnosis Algorithm Transcellular Shift • Recovery From DKA • Refeeding Syndrome • Acute Respiratory
Differential Diagnosis Algorithm ... Recovery From DKA ... • Vitamin D Deficiency ... Intake - Dietary deficiency ... #endocrinology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Disease • GH Deficiency ... • IGF-I Deficiency ... Panhypopituitarism Treatment ... #endocrinology
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
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