261 results
Hypocalcemia Laboratory Evaluation

Serum levels of PTH, phosphorus, 25-hydroxyvitamin D, and 1,25-dihydroxyvitamin D can help differentiate between
dihydroxyvitamin D can help differentiate ... receptor activating mutation ... Hyperparathyroidism #Diagnosis ... Endocrinology #Differential
Causes of Hypercalcemia due to increased Vitamin D levels
 • The BIG 3:
elasticum, CYP24A1 mutation ... infantile), SLC34A1 mutation ... VitaminD #causes #differential ... #diagnosis #endocrinology
Open Fractures: Mechanisms, Clinical Features and Complications
Gustilo-Anderson Classification:
 • Type I
   - Wound <
Fractures: Mechanisms, Clinical ... injuries, possible amputation ... Open #Fractures #Diagnosis
Chest Pain Differential Diagnosis and Clinical Features

#Diagnosis #ChestPain #Differential #Features #Comparison #Table
Chest Pain Differential ... Diagnosis and Clinical ... Features #Diagnosis ... #ChestPain #Differential
Hypercalcemia - Differential Diagnosis Algorithm
Primary Hyperparathyroidism
 • Adenoma
 • Hyperplasia
 • MEN 1 and 2A
Tertiary Hyperparathyroidism
Hypercalcemia - Differential ... Diagnosis Algorithm ... Calcium Receptor Mutation ... Hypercalcemia #Differential ... #Diagnosis #Algorithm
Hypocalcemia - Differential Diagnosis Algorithm - Low and High Phosphate
LOW PHOSPHATE
 - Low/NormaI PTH
Hypocalcemia - Differential ... Diagnosis Algorithm ... • Activating Mutation ... #Hypocalcemia #Differential ... #Diagnosis #Algorithm
Gaucher Disease 

Pathophsiology
 • Lysosomal storage disorder
 • Deficiency of ß-glucocerebrosidase
• Accumulation of glucosylceramide in macrophages
Diagnosis
in macrophages Diagnosis ... ß-glucocerebrosidase activity • Mutation ... in GBA1 gene Clinical ... Gauchers #Disease #Diagnosis
Distal Renal Tubular Acidosis
Distal RTA is the true Nephrogenic RTA and can be truly divided into
defect - ENaC mutation ... - SCNN mutation ... Acidosis #RTA #diagnosis ... #differential
Retinoblastoma: Pathogenesis and clinical findings
 • Sporadic mutation -> One allele of RB1 tumor suppressor gene
Pathogenesis and clinical ... findings • Sporadic mutation ... • Inherited mutation ... ophthalmology #diagnosis
Acute limb ischemia (ALI)

Rapid decrease in lower limb blood flow due to acute occlusion of peripheral
Critical Limb ischemia ... The twin Saints ... #CLI #heparin #amputation