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Genetic causes of craniofacial disorders

Genetic causes of craniofacial disorders - GenCFA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40561
Enrollment
100
Registered
2014-07-16
Start date
2014-12-31
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

congenital anomalies of the face and skull

Interventions

None listed

Sponsors

Genetica
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with congenital craniofacial anomalies, such as orofacial clefting, craniosynostosis, disorders of teeth development and syndromes with a distinct craniofacial phenotype.

Exclusion criteria

Exclusion criteria: Not applicable

Design outcomes

Primary

MeasureTime frame
Identification of new genetic causes of developmental craniofacial disorders.

Secondary

MeasureTime frame
Not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)