Genetic link between Fibrous Dysplasia and Intramuscular Myxoma in patients suffering from Mazabraud syndrome

Not Applicable

Recruiting

• Conditions: Mazabraud syndrome; Musculoskeletal - Other muscular and skeletal disorders

• Registration Number: ACTRN12616001371482
• Lead Sponsor: Hollywood Private Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-10-04
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 4

Inclusion Criteria

Patients with confirmed diagnosis of both Intramuscular Myxoma and Fibrous Dysplesia (which is known as Mazabraud syndrome)

Exclusion Criteria

Not provided

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Finding common genetic mutations in patient suffering from both Fibrous Dysplasia and Intramuscular Myxoma, known as Mazabraud syndrome [One blood sample will be taken.]

Secondary Outcome Measures

Name	Time	Method
Knowing common genetic mutations will help in distinguishing fibrous dysplesia from malignant tumours [One blood sample will be taken.];Detecting those mutations which lead to fibrous dysplasia in those who are suffering from multiple intramuscular myxoma[One blood sample will be taken.]