The phenotype/genotype correlations in children with coeliac disease.

The phenotype/genotype correlations in children with coeliac disease. - Phenotype/genotype study in coeliac disease

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON30380

Enrollment

800

Registered

2006-10-31

Start date

2007-07-14

Completion date

Unknown

Last updated

2024-06-18

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

Conditions

gluten intolerance gluten sensitive enteropathy

Interventions

None listed

Eligibility

Age

2 Years to 17 Years

Inclusion criteria

Inclusion criteria: (1) Included: -Born in The Netherlands -Diagnosis of coeliac disease based on at least 1 biopsy of the small intestine, showing the characteristic appearance of coeliac disease (villous atrophy, crypt hyperplasia, inflammatory infiltration). -Age at diagnosis (diagnostic biopsy of the small intestine) between 0 to 14 years. -Clinical data already collected. (2) Informed consent obtained for present study.

Exclusion criteria

Exclusion criteria: No informed consent obtained for present study.

Design outcomes

Primary

Measure	Time frame
An association will be investigated between clinical information (age at onset, clinical data, associated diseases) and variants of candidate genes of coeliac disease.	—

Secondary

Measure	Time frame
nvt	—

Countries

Netherlands

Outcome results