This is the first study with a real diagnostic and prognostic focus in prenatal. In addition to this innovative aspect, the identification of cryptic imbalances in fetuses with malformative syndrome would be an invaluable resource for the identification of new genes involved in development, as is already the case for postnatal studies. This research aims to: 1. to test the feasibility of this protocol, ie the practical application of this new technology in the context of prenatal diagnosis, 2. demonstrate and evaluate the possible involvement of cryptic chromosomal abnormalities in fetuses with a thick neck associated with other malformations and recruited on the strict criteria mentioned above, 3. assist in the diagnosis of these fetuses and genetic information for their families, 4. identify new regions of the genome potentially involved in the occurrence of congenital malformations.
Study Type
OBSERVATIONAL
Enrollment
200
Hôpital Jeanne de Flandre - CHRU de Lille
Lille, France
Number of patient with Ultrasound call signs (thick neck and / or any other organ concerned)
Time frame: During the first trimester of pregnancy
CGH-array analysis
CGH-array result: normal, deletion or duplication, de novo or inherited, size, type and number of genes involved
Time frame: During the first trimester of pregnancy
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.