Follow up and Observation of Charcot Marie Tooth Disease in Families

This study has been completed.
Information provided by:
Hadassah Medical Organization Identifier:
First received: September 7, 2005
Last updated: November 6, 2006
Last verified: August 2005
The study is aimed to test the hypothesis that there is anticipation in CMT

Charcot-Marie-Tooth Disease

Study Type: Observational
Study Design: Observational Model: Defined Population
Time Perspective: Longitudinal
Official Title: Clinical and Genetic Features of Familial Neuropathy

Resource links provided by NLM:

Further study details as provided by Hadassah Medical Organization:

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

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

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

Exclusion Criteria:

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00149045

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

No publications provided Identifier: NCT00149045     History of Changes
Other Study ID Numbers: 920010132-HMO-CTIL
Study First Received: September 7, 2005
Last Updated: November 6, 2006
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:
familial peripheral Neuropathy Anticipation

Additional relevant MeSH terms:
Charcot-Marie-Tooth Disease
Hereditary Sensory and Motor Neuropathy
Nerve Compression Syndromes
Tooth Diseases
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Nervous System Diseases
Neurodegenerative Diseases
Neuromuscular Diseases
Peripheral Nervous System Diseases
Stomatognathic Diseases
Congenital Abnormalities
Nervous System Malformations
Polyneuropathies processed this record on November 27, 2015