82 results
Manifestations of IgG4-related disease by organ system.
 The most common primary disease features are indicated in
of IgG4-related disease ... features are indicated ... Organs #Systems #Diagnosis ... #Hematology #Signs ... #Symptoms
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
Rheumatoid Arthritis Summary
MCP and PIP Involvement, Spares DIP, Carpal Tunnel, Sicca Syndrome, Epi/Scleritis, Heart Disease, Rheumatoid
Rheumatoid Nodules, Pulmonary ... Disease and ILD ... Arthritis #RA #diagnosis ... #rheumatology # ... signs #symptoms
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
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
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
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
Systemic Sclerosis (Scleroderma)
Multi-system autoimmune disease characterized by vasculopathy and progressive fibrosis of skin and internal organs
3
Multi-system autoimmune disease ... and Symptoms: ... ), PAH (pulmonary ... Scleroderma #SSc #rheumatology ... #diagnosis #signs
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