Genetic Linkage Study of Idiopathic Talipes Equinovarus (ITEV) (Clubfoot)
NCT00474344 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 370
Last updated 2022-05-18
Summary
The goal of this study is to identify and characterize the genetic loci causing idiopathic talipes equinovarus (clubfoot).
The hypothesis is that a few genes account for a substantial fraction of ITEV and that these genes can be identified in defined populations. Towards this goal, in preliminary studies, Dr. Hecht's group has identified two genes, NAT2 and CASP10, which demonstrate evidence for linkage and association to ITEV.
Conditions
- Clubfoot
Sponsors & Collaborators
-
National Institutes of Health (NIH)
collaborator NIH -
Shriners Hospitals for Children
collaborator OTHER -
University of British Columbia
lead OTHER
Principal Investigators
-
Christine Alvarez, MD · University of British Columbia
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-08-31
- Primary Completion
- 2010-12-31
- Completion
- 2013-08-31
Countries
- United States
- Canada
Study Locations
More Related Trials
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Project
NCT00474331 ·Status: SUSPENDED
-
Establishing the Genetic Profile of Multiple Hereditary Exostoses (HME) in Families of BC
NCT00473850 ·Status: TERMINATED
-
Clubfoot DNA Repository
NCT00607191 ·Status: COMPLETED
-
Defining the Genetic Etiology of Suppurative Lung Disease in Children and Adults
NCT04702243 ·Status: COMPLETED
-
Studies of Hereditary Hemorrhagic Telangiectasia
NCT00004648 ·Status: COMPLETED
-
Experiences of Genetics Patients With Visible Abnormalities Who Facilitate Teaching in Genetics Clinics
NCT00341718 ·Status: COMPLETED
-
Optimal Approach for Analysis of Case-Control Genetic Association Studies
NCT00241709 ·Status: COMPLETED
-
Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population
NCT00341068 ·Status: TERMINATED
-
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2
NCT01193088 ·Status: RECRUITING
-
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq)
NCT05354622 ·Status: RECRUITING
-
Study of Genetic Risk Factors for Spina Bifida and Anencephaly
NCT00031122 ·Status: UNKNOWN
-
Study of Heritable Connective Tissue Disorders
NCT00001641 ·Status: COMPLETED
-
Genetics of Neural Tube Defects
NCT01253746 ·Status: UNKNOWN
-
Genetics of Familial Testicular Cancer
NCT00342537 ·Status: COMPLETED
-
Genetics of Spina Bifida and Anencephaly
NCT00636233 ·Status: COMPLETED
-
Suitability of Some Data Quality Controls Thresholds for Genetic Association Studies of Admixed Population
NCT02770001 ·Status: WITHDRAWN
-
Candidate Gene Association Study With Injury in Elite Male Youth Football Players
NCT04952662 ·Status: COMPLETED
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Genetics of Differences of Sex Development and Hypospadias
NCT03102554 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex
NCT00001452 ·Status: COMPLETED
-
Genetic Predisposition in Cerebral Palsy
NCT05317234 ·Status: RECRUITING ·Phase: NA
-
Clinical Presentation of Genetic Disorders in Patients Attending Genetic Outpatient Clinic of Assiut University Children Hospital
NCT05888155 ·Status: UNKNOWN
-
Study to Estimate How Common it is to Have Genetic Variants Associated With NAFLD
NCT04494360 ·Status: COMPLETED
-
Clinical and Genetic Studies of VACTERL Association
NCT00766571 ·Status: COMPLETED