Status:
COMPLETED
Characterization of At-risk Population for Pre-sacral Tumor in CURRARINO Syndrome
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Conditions:
CURRARINO Syndrome
Sacrococcygeal Teratoma
Eligibility:
All Genders
Brief Summary
Contribute to support hypothesis of relationships between genes involve in oncogenesis and those involve in embryological development.
Detailed Description
CURRARINO syndrome (CS) (OMIM 176450) is a rare congenital disease described in 1981, as the association of, at least, three main clinical features: typical sacral malformation (sickled-shape sacrum o...
Eligibility Criteria
Inclusion
- At least 1 out of the 4 major signs of CURRARINO syndrome:
- Sacral agenesis
- Hindgut malformation or chronic constipation
- Presacral tumor and/or
- TETHECORD syndrome and/or lipoma of the filum or the conus
- Anomaly genotyping HLXB9 without clinical expression
Exclusion
- \- Opposition to sign informed consent agreement
Key Trial Info
Start Date :
June 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2011
Estimated Enrollment :
57 Patients enrolled
Trial Details
Trial ID
NCT00780117
Start Date
June 1 2008
End Date
December 1 2011
Last Update
July 26 2012
Active Locations (1)
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1
Hôpital Necker-Enfants Malades Pediatric Surgery Department
Paris, France, 75015