Screening an Orthopedic Population for Mildly-affected Individuals With Morquio Syndrome A and Maroteaux-Lamy Syndrome

NCT ID: NCT01961518

Last Updated: 2015-08-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

17 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-10-31

Study Completion Date

2015-05-31

Brief Summary

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The purpose of this study is to identify patients with Morquio syndrome type A (MPS IVA) and Maroteaux-Lamy syndrome (MPS VI) who may have been missed or misdiagnosed due to atypical clinical features, a milder course, and/or negative urine screening. We will recruit participants who have certain hip and/or joint problems that could potentially be caused by one of these two genetic conditions through a chart review process conducted at Shriners Hospital for Children in Greenville, SC. Diagnostic testing will be performed for each participant to determine if he or she is affected by one of these two conditions. Results will be disclosed to all participants and their legal guardians, and appropriate follow up will be recommended for those who are found to have abnormal results.

Detailed Description

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Conditions

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Morquio Syndrome A Maroteaux Lamy Syndrome MPS IVA MPS VI

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Eligible participants must currently receive care in the Shriners Hospitals for Children system, and therefore, will be under 19 years of age.
* Eligible participants must have one of the following diagnoses: bilateral Legg-Calve-Perthes disease, bilateral hip dysplasia, multiple joint pain, unidentified skeletal dysplasia
* Eligible participants (or legal guardian) must be able and willing to sign informed consent/assent in English or Spanish.

Exclusion Criteria

* Participants with one or more or the above inclusion diagnoses who have a specific etiologic diagnosis will not be eligible to participate in this study.
* If we are unable to obtain the necessary specimens, the participant will be removed from the study.
Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shriners Hospitals for Children

OTHER

Sponsor Role collaborator

BioMarin Pharmaceutical

INDUSTRY

Sponsor Role collaborator

Greenwood Genetic Center

OTHER

Sponsor Role lead

Responsible Party

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R. Curtis Rogers

Senior Clinical Geneticst

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Richard Curtis Rogers, MD

Role: PRINCIPAL_INVESTIGATOR

Greenwood Genetic Center

Locations

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Greenwood Genetic Center

Greenville, South Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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GGC001

Identifier Type: -

Identifier Source: org_study_id

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