Trials / Terminated
TerminatedNCT01907425
Prenatal Molecular Characterisation by CGH+SNP-ARRAY of Supernumerary Marker Chromosomes and de Novo Apparently Balanced Reciprocal Translocations
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Centre Hospitalier Universitaire Dijon · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
In the prenatal period, les supernumerary marker chromosomes (SMC) and de novo apparently balanced reciprocal translocations are revealed by foetal karyotyping, which does not always make it possible to determine whether the anomaly is balanced or not and does not reveal uniparental disomy. The presence of these chromosomal rearrangements raises a difficult question for genetic counselling during pregnancy because of the risk of intellectual deficiency in the foetus. CGH+SNP-Array can provide information concerning 1) the balanced or not nature of these translocations 2) the presence or not of euchromatin in the SMC 3) the presence or not of uniparental disomy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Blood samples |
Timeline
- Start date
- 2013-08-30
- Primary completion
- 2017-05-22
- First posted
- 2013-07-25
- Last updated
- 2024-02-21
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT01907425. Inclusion in this directory is not an endorsement.