Follow up and Observation of Charcot Marie Tooth Disease in Families

This study has been completed.

Sponsored by:	Hadassah Medical Organization
Information provided by:	Hadassah Medical Organization
ClinicalTrials.gov Identifier:	NCT00149045

Purpose

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

Condition
Charcot-Marie-Tooth Disease

Genetics Home Reference related topics: Charcot-Marie-Tooth disease familial encephalopathy with neuroserpin inclusion bodies hereditary neuropathy with liability to pressure palsies

MedlinePlus related topics: Charcot-Marie-Tooth Disease Tooth Disorders

U.S. FDA Resources

Study Type:	Observational
Study Design:	Natural History, Longitudinal, Defined Population, Retrospective/Prospective Study
Official Title:	Clinical and Genetic Features of Familial Neuropathy

Further study details as provided by Hadassah Medical Organization:

Study Start Date:	November 2001
Estimated Study Completion Date:	August 2005

Eligibility

Ages Eligible for Study:	8 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

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

Exclusion Criteria:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: 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

More Information

Study ID Numbers:	920010132-HMO-CTIL
Study First Received:	September 7, 2005
Last Updated:	November 6, 2006
ClinicalTrials.gov Identifier:	NCT00149045
Health Authority:	Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:

familial peripheral Neuropathy Anticipation

Study placed in the following topic categories:

Tooth Diseases
Nervous System Malformations
Roussy Levy hereditary areflexic dystasia
Charcot-Marie-Tooth Disease
Polyneuropathies
Neurodegenerative Diseases
Nerve Compression Syndromes
Tomaculous neuropathy

Heredodegenerative Disorders, Nervous System
Neuromuscular Diseases
Genetic Diseases, Inborn
Peripheral Nervous System Diseases
Hereditary Motor and Sensory Neuropathies
Stomatognathic Diseases
Congenital Abnormalities
Charcot Marie Tooth disease

Additional relevant MeSH terms:

Nervous System Diseases

ClinicalTrials.gov processed this record on January 16, 2009