NCT02862834

Screening for Genes in Patients With Poikiloderma

Towards an Improvement in Diagnosis and Genetic Counselling in Syndromic Poikiloderma

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 39 (actual)
• Sponsor: Centre Hospitalier Universitaire Dijon · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

In the context of this study, the investigators wish to take advantage of high-throughput genetic techniques (microarray and high-throughput exome sequencing) to identify new genes implicated in syndromic poikiloderma so as to improve the diagnostic decision tree in these syndromes, opportunities for genetic counselling for patients and their families and the follow-up of patients, notably with regard to the risk of tumours. This study will make it possible to identify new genes implicated in syndromic poikiloderma and improve the diagnostic strategy proposed to patients with these syndromes, and to propose to patients a confirmed diagnosis, appropriate follow-up, notably with regard to the risk of tumours, genetic counselling to families and eventually an antenatal diagnosis to couples who would like to have one for future pregnancies. The identification of new genetic causes of syndromic poikiloderma will also make it possible to complete the current classification of these syndromes

Conditions

• Poikiloderma

Interventions

Type	Name	Description
GENETIC	High-throughput exome sequencing

Timeline

• Start date: 2013-05-01
• Primary completion: 2015-09-01
• First posted: 2016-08-11
• Last updated: 2026-03-12

Locations

1 site across 1 country: France