51 results
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... Peds #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... additions, for diagnosing ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Peds #Pediatrics #Table ... #NICU #Genetics
Modified Allen’s Test before doing a radial ABG #Clinical #Diagnosis #Allen #Test #RebelEM
’s Test before doing ... a radial ABG #Clinical ... #Diagnosis #Allen
Etiologies of Hypoaldosteronism

Hyporeninemic Hypoaldosteronism (Low Renin, Low Aldosterone)
 - Diabetic Nephropathy 
 - NSAIDs
Non-Hyporeninemic Hypoaldosteronism (Normal
insufficiency - Critical ... illness - Genetic ... Sulfamethoxazole - Genetic ... #Differential #Diagnosis ... Aldosterone #Comparison #Table
Diverticulosis and Angiodysplasia - Pathophysiology and Clinical Features

#Diverticulosis #Angiodysplasia #Pathophysiology #diagnosis #algorithm
Angiodysplasia - Pathophysiology ... and Clinical Features ... Angiodysplasia #Pathophysiology ... #diagnosis #algorithm
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Erythroderma - Diagnostic ... Algorithm. ... Pathophysiology: ... Histamine 4) Skin-homing ... T-cells #Diagnosis
Irritable Bowel Syndrome (IBS) - Pathophysiology, Diagnosis and Management Algorithm
Risk factors: Previous acute enteric infection, Female
Syndrome (IBS) - Pathophysiology ... , Diagnosis and ... Management Algorithm ... depression, Poor coping ... #Diagnosis #Management
Summary of types of haemolytic anaemia. Visit gramproject.com for more medical diagrams, tables and flowcharts for
medical diagrams, tables ... #diagnosis #clinical ... #differential #algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Summary flowchart for investigating suspected pulmonary embolism. Visit gramproject.com for more medical diagrams, tables and flowcharts
medical diagrams, tables ... #diagnosis #algorithm ... em #pulmonary #clinical