Exostoses, Multiple Hereditary Clinical Trial
Official title:
Establishing the Genetic Profile of Multiple Hereditary Exostoses (HME) in Families of BC
The purpose of this study is to establish the genetic profile of families in British Columbia with HME.
The purpose of this study is to establish the genetic make-up of families and patients with
HME. This will occur as the patient presents to a regular clinic visit. Dr. Alvarez will be
introduced to interested patients and their parent(s) and a brief discussion about the
project will occur. If the patient and their direct family are interested they will be
entered into the study. This will involve interviewing the patients and their direct family.
This interview will take about 1 hour. We are interested in identifying all affected family
members as far up the family tree as possible. We ask that the idea of the study be
introduced to extended family members by the participating family members and then have them
call Dr. Alvarez to set up an appointment. Each available member will be interviewed and a
physical exam done to determine the location of osteochondromas. In addition, Xrays will be
done to determine the location of all osteochondromas. All Xrays will be reviewed. No new
ones will be taken unless it is part of the patient's routine care.
To complete the genetic work up DNA analysis will be done on all available family members.
This will entail obtaining a blood sample from each family member willing to partake in the
study. These blood samples will be used only for the purpose of identifying abnormalities in
the genes related to osteochondromas. The blood samples will be taken at British Columbia's
Children's Hospital and processed there. DNA samples will be kept confidential.
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Observational Model: Case-Only, Time Perspective: Retrospective
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