An observational study in Leukodystrophy and Leukoencephalopathy, sponsored by National Human Genome Research Institute (NHGRI). Completed at 1 site in United States. Open to participants aged 1 Month to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-08-03.
Sponsored by National Human Genome Research Institute (NHGRI) · Observational
Background:
Objectives:
Eligibility:
Any individual with a known or suspected leukodystrophy is eligible to participate in this protocol, including
Design:
The following tests will be conducted as part of standard clinical care:
The following studies may be performed as part of participation in the research:
Genetic white matter disorders (leukodystrophies) are estimated to have an incidence of 1:5000 live births. As many as 50% of patients with white matter disease remain undiagnosed after conventional neuroimaging, biochemical and genetic testing, and therefore have unclassified leukodystrophies. Moreover, the mechanisms of disease in many leukodystrophies of known cause are very poorly understood: many are systemic abnormalities that manifest only in white matter. The purpose of this study is to: (a) define novel homogeneous groups of patients with leukodystrophy and work toward finding the cause of these disorders and (b) establish disease mechanisms in selected classified leukodystrophies. In order to achieve these goals, patients with leukodystrophy will be analyzed by clinical, neurophysiological, biochemical and genetic means. For goal (a), patients would have been diagnosed as having an unclassified leukodystrophy or no known cause of their leukodystrophy at outside centers. At the Clinical Center, such patients will undergo a series of neuropsychological, blood, urine, spinal fluid, radiological, and peripheral tissue pathological tests. Some of these tests will be part of a standard battery while others will be tailored to individual patients. For goal (b), selected leukodystrophies with a defined genetic cause will be selected for further mechanistic study, using clinical and laboratory tools to establish increased understanding of the underlying pathophysiology. It is hoped that the present study will help clarify the nosology of the leukodystrophies and significantly advance our understanding of the pathogenesis of these diseases.
EXCLUSION CRITERIA:
This study is completed, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.
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National Human Genome Research Institute (NHGRI)