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Molecular studies in a multigenerational family with gastro-esophageal reflux disease (GERD)

Completed
Conditions
GERD
heartburn
10018018
10017977
Registration Number
NL-OMON35981
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
23
Inclusion Criteria

- Affected family members and all adult unaffected family members will be asked to participate. Family members are considered to be affected either if a diagnosis of GERD has been made by a physician (usually a [pediatric] gastroenterologist), if additional investigations such as pH/impedance measurements or gastroesophageal endoscopies show evidence for GERD, or if anti-reflux surgery has been performed in the past. GERD is considered as a dichotomous trait in this study.
- Informed consent is needed to be included. Informed consent will be asked for by the parents when children are under the age of 12 years. At present there is only a single affected child (8 yrs) in this family.

Exclusion Criteria

Insufficient understanding of the purpose and risks of the study.

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary outcome is linkage to one or more chromosome regions and<br /><br>idenfication of associated gene(s) in the GERD family. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The secondary outcome will consist of a thorough description of the clinical<br /><br>characteristics, the phenotype, of patients with GERD in this family. </p><br>
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