CompletedNCT04691414

Retrospective Study Using Next Generation Sequencing (NGS) on Biological Samples to Improve Genetic Counseling for Patients With Previously Explored Craniofacial Midline Defects.

Studying OBSOLETE: Congenital nasal pyriform aperture stenosis with holoprosencephaly

Last synced from ClinicalTrials.gov May 10, 2026

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Key facts

Sponsor: Rennes University Hospital
Principal Investigator: Alinoë LAVILLAUREIX
CHU Rennes
Intervention: NGS(genetic)
Enrollment: 33 enrolled
Eligibility: All sexes
Timeline: 2021 – 2021

Study locations (1)

CHU Rennes, Rennes, France

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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