French Digestive Polyposis Cohorte Family Adenomatous Polyposis With APC and MYH Gene Mutations , Cowden's Disease With PTEN Gene Mutation, Peutz Jeghers Disease With STK 11 Gene Mutation ,juvénil Polyposis With SMAD 4 Gene Mutation , Serrated and Hyperplastic Polyposis

N/AUnknownNCT01987518

Hôpital Edouard Herriot350 enrolled

Overview

French cohorte about polyposis digestive diseases

Family Adenomatous Polyposis APC and MYH Genes Peutz Jeghers Disease Cowden Disease Festooned polyposis Juvenile polyposis Hyperplastic polyposis

Study Type

OBSERVATIONAL

Enrollment

350

Conditions

Quality of Life

Interventions

Procedure surgery behavioral and genetic diagnosisOTHER

Observational Study

quality of life after different type of surgeryPROCEDURE

Eligibility

Sex: ALLMin age: 12 YearsMax age: 90 Years

Medical Language ↔ Plain English

Inclusion Criteria: * APC Gene mutation * MYH Homozygote mutation * COWDEN Disease with PTEN gene mutation * Peutz Jeghers Disease with STK 11 gene mutation * Juvenile polyposis with SMAD 4 gene mutation Exclusion Criteria: * heterozygote MYH Gene Mutation

Locations (1)

Hopital Edouard Herriot

Lyon, Auvergne-Rhône-Alpes, France

RECRUITING

Outcomes

Primary Outcomes

genetic diagnosis or over 50 polyps in the stomach in the duodenum or in the colon

Time frame: 10 years

Data from ClinicalTrials.gov

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