92 results
Femoral Head Fracture: Pathogenesis and clinical findings
 • Posterior hip dislocation -> Impaction force from femoral
Pathogenesis and clinical ... onto lateral hip Signs ... #msk #diagnosis ... #pathophysiology ... #signs #symptoms
Pott's Disease in Tuberculosis - Diagnosis and Management Summary
Epidemiology:
 - Typically from TB endemic areas
 -
Pott's Disease in ... extrapulmonary cases Clinical ... Signs/Symptoms: ... pulmonary TB PE ... decreased reflexes Pathophysiology
Fat Embolism Syndrome
Trauma to the long bone or pelvis accounts for —9096 of cases. The diagnosis
stabilization of fractures ... Pathophysiology ... onset widespread pulmonary ... FES is a clinical ... #Signs #Symptoms
Cardiac Amyloid - Diagnosis, Signs, Symptoms and Management

Clinical Presentation
- exertional dyspnea
- peripheral edema
- exertional syncope
- peripheral
, Signs, Symptoms ... and Management ... Clinical Presentation ... - conduction disease ... #Signs #Symptoms
Common Biliary Diseases seen in the Emergency Room - Comparison Table:

Clinical Features, Labs, Imaging and Treatment

#Diagnosis
Common Biliary Diseases ... : Clinical Features ... and Treatment #Diagnosis ... #Management #BiliaryDiseases ... #Table #Approach
Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings

Pars interarticularis stress fracture (spondylolysis) - most frequently in the
Pathogenesis and Clinical ... interarticularis stress fracture ... Spondylolisthesis #MSK #diagnosis ... #pathophysiology ... #signs #symptoms
Wilson's Disease - Pathogenesis and Clinical Features

#Wilsons #Disease #Pathophysiology #signs #symptoms #diagnosis #copper
Pathogenesis and Clinical ... Features #Wilsons ... #Disease #Pathophysiology ... #signs #symptoms ... #diagnosis #copper
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... sleep apnea, cor pulmonale
Gaucher Disease 

Pathophsiology
 • Lysosomal storage disorder
 • Deficiency of ß-glucocerebrosidase
• Accumulation of glucosylceramide in macrophages
Diagnosis
Gaucher Disease ... Pathophsiology ... in GBA1 gene Clinical ... #Diagnosis #Signs ... #Symptoms
Sarcoidosis 
Non-caseating granulomas (Composed of T-helper & inflammatory cells) 
Clinical:
 • Disease fatal in 10% of
inflammatory cells) Clinical ... : • Disease fatal ... #Sarcoidosis #Diagnosis ... #Symptoms #Signs ... #Pulmonary