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Follow up and Observation of Charcot Marie Tooth Disease in Families

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ClinicalTrials.gov Identifier: NCT00149045
Recruitment Status : Completed
First Posted : September 8, 2005
Last Update Posted : November 7, 2006
Sponsor:
Information provided by:
Hadassah Medical Organization

Brief Summary:
The study is aimed to test the hypothesis that there is anticipation in CMT

Condition or disease
Charcot-Marie-Tooth Disease

Study Type : Observational
Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Retrospective/Prospective
Official Title: Clinical and Genetic Features of Familial Neuropathy
Study Start Date : November 2001
Study Completion Date : August 2005






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Ages Eligible for Study:   8 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:Patients with Genetically confirmed CMT 1a disease -

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00149045


Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel, 91120
Sponsors and Collaborators
Hadassah Medical Organization
Investigators
Principal Investigator: Israel Steiner, MD Hadssah University Hospital, Department of Neurology

ClinicalTrials.gov Identifier: NCT00149045     History of Changes
Other Study ID Numbers: 920010132-HMO-CTIL
First Posted: September 8, 2005    Key Record Dates
Last Update Posted: November 7, 2006
Last Verified: August 2005

Keywords provided by Hadassah Medical Organization:
familial peripheral Neuropathy Anticipation

Additional relevant MeSH terms:
Charcot-Marie-Tooth Disease
Nerve Compression Syndromes
Hereditary Sensory and Motor Neuropathy
Tooth Diseases
Stomatognathic Diseases
Nervous System Malformations
Nervous System Diseases
Heredodegenerative Disorders, Nervous System
Neurodegenerative Diseases
Polyneuropathies
Peripheral Nervous System Diseases
Neuromuscular Diseases
Congenital Abnormalities
Genetic Diseases, Inborn