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diagnosis algorithm iem inbornerrors management neonatology nicu pediatrics aflp allergy ammonia anemia approach bile biliary classification duct fatty hemeonc hemophagocytic
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
A table of lab ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table ... #NICU #Genetics
Causes of Neutrophilia - Increased Neutrophils - Differential Diagnosis Algorithm Infection • Bacterial • Abscess • Viral Medications
Causes of Neutrophilia ... Neutrophils - Differential ... Emotional stimuli • Metabolic ... disorders • Asplenia ... #Hematology
Overall Approach to Anemia - Differential Diagnosis Algorithm Blood Loss • Acute Bleed - Normocytic / Normochromic
Approach to Anemia - Differential ... • RBC Metabolism ... Disorder - Acquired ... Diagnosis #Algorithm #Causes ... #Hematology
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
and decreased metabolism ... Inherited Urea Cycle Disorders ... Reye syndrome (Peds ... deficiency #Ammonia #Pathophysiology ... Hyperammonemia #Differential
Acute Fatty Liver of Pregnancy (AFLP) Pathophysiology: • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... free fatty acid metabolism ... = nonspecific (nausea ... infiltration) Differential ... Liver #Pregnancy #hepatology
Approach to Elevated Tryptase - Differential Diagnosis Framework The DDx of elevated tryptase can be broken down
Elevated Tryptase - Differential ... Eosinophilic GI Disorders ... 4th pass = Genetic ... #Tryptase #Differential ... #Diagnosis #hematology
Bile Duct Paucity - Differential Diagnosis • Genetic: Alagille syndrome, Trisomy 21, Williams syndrome, Peroxisomal disorders
Duct Paucity - Differential ... Diagnosis • Genetic ... • Metabolic: α1 ... Paucity #biliary #hepatology ... #Differential #
Rhabdomyolysis - Differential Diagnosis Framework Rhabdomyolysis = Destruction of skeletal muscle with leakage of contents into circulation.
Compression • Genetic ... Glycogenolysis, Lipid metabolism ... Mitochondrial disorders ... #Diagnosis #Causes ... #nephrology #table
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... Familial) HLH: - Genetic ... Pathophysiology ... malignancy, autoimmune disorder ... Diagnosis #Management #Hematology
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