SMN Copy Number Distribution in Mali, West Africa
NCT01059240 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 701
Last updated 2019-12-05
Summary
Background:
* Spinal muscular atrophy (SMA) is a degenerative and incurable neuromuscular disorder that is caused by mutations in the survival motor neuron gene, SMN1, found on chromosome 5. It is the leading inherited cause of infant mortality. SMA carriers (those who have the genetic mutation but do not have the disease) are often unaware of their status until they are tested.
* Researchers have been studying the prevalence of SMA carriers in the general population, but most of the information collected has come from populations within the United States, Europe, and Asia. Very few studies have been performed in Africa. Furthermore, this information does not provide much information regarding carrier frequency based on ethnic background and ancestry. To address this problem, researchers are interested in studying the prevalence of the SMA genetic mutation in the sub-Saharan nation of Mali.
Objectives:
\- To collect blood samples for use in studying genetic data related to spinal muscular atrophy.
Eligibility:
* Healthy volunteers who are at least 18 years of age.
* Volunteers will be of Malian ancestry and nationality.
Study Location:
-\<TAB\>Bamako, Mali, West Africa
Design:
* The study will first collect blood samples from a small group of volunteers to run initial SMA carrier testing and resolve any technical difficulties before continuing with the study.
* Participants will complete questionnaires about their personal and family medical history, including questions about illnesses, stillborns, and miscarriages, and then will provide blood samples for genetic research and testing.
Conditions
Sponsors & Collaborators
-
National Institute of Neurological Disorders and Stroke (NINDS)
lead NIH
Principal Investigators
-
Kenneth H Fischbeck, M.D. · National Institute of Neurological Disorders and Stroke (NINDS)
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-01-21
- Completion
- 2017-05-18
Countries
- Mali
Study Locations
More Related Trials
-
Genetic and Blood Biomarkers in Neurological and Neuromuscular Diseases
NCT02780531 ·Status: COMPLETED
-
Genetic Characterization of Individuals With Limb Girdle Muscular Dystrophy
NCT00457912 ·Status: COMPLETED
-
Clinical and Molecular Studies in Families With Inherited Eye Disease
NCT02771236 ·Status: RECRUITING
-
Genetic Characterization of Movement Disorders and Dementias
NCT02014246 ·Status: RECRUITING
-
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
NCT00136630 ·Status: COMPLETED
-
Clinical and Laboratory Study of Methylmalonic Acidemia
NCT00078078 ·Status: RECRUITING
-
Genetic Analysis of Hereditary Disorders of Hearing and Balance
NCT00023049 ·Status: COMPLETED
-
Clinical Importance of Carrier Status of Recessive Gene Mutations in Myopathy (CICS)
NCT02897921 ·Status: UNKNOWN
-
Genetics of Inherited Eye Disease
NCT02471287 ·Status: RECRUITING
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING
-
Characterization of Angelman Syndrome
NCT00296764 ·Status: COMPLETED
-
Genetics of Familial and Sporadic ALS
NCT00821132 ·Status: COMPLETED
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Cause and Pathogenesis of Neurometabolic Disorders
NCT00016562 ·Status: COMPLETED
-
Study to Identify the Genetic Variations Associated With Phantom Limb Pain
NCT01462448 ·Status: COMPLETED
-
Genetic Studies of Lysosomal Storage Disorders
NCT00001215 ·Status: ENROLLING_BY_INVITATION
-
GNAO1 Natural History Study
NCT04950946 ·Status: UNKNOWN
-
Genetics of Progressive Multifocal Leukoencephalopathy and Acquired Immunodeficiency Syndrome
NCT00342602 ·Status: COMPLETED
-
Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation
NCT02089789 ·Status: RECRUITING
-
Characteristics of Episodic Ataxia Syndrome
NCT00266760 ·Status: COMPLETED
-
Genetic Identification of Monogenic Disorders in Early-onset Stroke Using Targeted Next Generation Sequencing Panel
NCT04485598 ·Status: COMPLETED
-
A Natural History Study of the Gangliosidoses
NCT00668187 ·Status: RECRUITING
-
Genetics of Charcot-Marie-Tooth Dystrophy and Related Diseases
NCT04967716 ·Status: UNKNOWN
-
Natural History Study of GEMIN-5 Related Neurodevelopmental Disorder
NCT06776341 ·Status: RECRUITING
-
Transitional Life Events in Patients With Friedreich's Ataxia: Implications for Genetic Counseling
NCT00056186 ·Status: COMPLETED