Genetic Analysis of Hereditary Non-Syndromic Oral Clefts

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00340626

Enrollment

690

Registered

2006-06-21

Start date

1997-08-31

Completion date

2020-03-12

Last updated

2020-03-13

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

Conditions

Hereditary Oral Clefts

Keywords

Linkage Analysis, Genotyping, Birth Defects, Family Study, Positional Cloning

Brief summary

In a collaborative effort with the IBN AL-NAFEES Hospital (Damascus, Syrian Arab Republic), individuals from multiplex families determined to have hereditary oral clefts will be studied. The purpose of this study is to identify the gene(s) involved in heritable oral clefts by linkage analysis and gene mapping strategies. Characterization of genes involved in inherited oral clefts could provide important insight into the inheritance and pathogenesis of this disease.

Detailed description

In a collaborative effort with the IBN AL-NAFEES Hospital (Damascus, Syrian Arab Republic), individuals from multiplex families determined to have hereditary oral clefts will be studied. Healthy Syrian individuals with no family history of oral clefts will also be enrolled as a comparison group. The purpose of this study is to identify the gene(s) involved in heritable oral clefts by linkage analysis and gene mapping strategies. Characterization of genes involved in inherited oral clefts could provide important insight into the inheritance and pathogenesis of this disease. All families are enrolled into the study by our Syrian collaborators (under Ethics Board approval from the IBN AL-NAFEES Hospital) and only coded phenotype data and coded biospecimens are ever received at the NIH.

Interventions

None listed

Study design

Observational model

FAMILY_BASED

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* INCLUSION CRITERIA: Enrollment in this study will be limited to individuals with non-syndromic unilateral or bilateral cleft lip with or without cleft palate and their unaffected relatives, from families which meet the following criteria: 1. A cluster of 2 or more affected first degree relatives, such as a parent and two offspring or 2 siblings, or 2. The occurrence of oral clefts in each of 2 generations in either the proband's paternal or maternal lineages. 3. The occurrence of oral clefts in 2 or more cousins (up to second cousins) The subject population is comprised of probands and their families previously examined at the IBN-AL NAFEES Hospital or at other hospitals and clinics in the Syrian Arab Republic as well as healthy controls from the same population. Consent documents are in Arabic language for non-English-speaking subjects

Exclusion criteria

Individuals unable to provide consent, except for cases who are children and mentally impaired persons with consenting parents or guardians.

Design outcomes

Primary

Measure	Time frame	Description
Identification of genetic risk variants for oral clefts	Ongoing	To identify and characterize genes responsible for non- syndromic and syndromic oral clefts by genetic family studies including linkage analysis, association analysis, positional cloning, evaluation of candidate genes, and eventual evaluation of mutations in identified genes.

Countries

Syria

Outcome results