RecruitingNCT03639285

Natural History, Diagnosis, and Outcomes for Leukodystrophies


Sponsor

University of Utah

Enrollment

600 participants

Start Date

Jan 19, 2007

Study Type

OBSERVATIONAL

Conditions

Summary

The goals of this protocol is to diagnose, care for, and understand the clinical histories and outcomes of people with leukodystrophies.


Eligibility

Inclusion Criteria3

  • evidence by clinical exam, radiological findings, and/or testing, of an inherited leukodystrophy.
  • be able to travel to the leukodystrophy clinic (at Primary Children's Hospital, Salt Lake City, Utah);
  • be able to tolerate a general physical exam, and a neurological exam.

Exclusion Criteria4

  • unable to be evaluated at the University of Utah Hospital or Primary Children's Hospital;
  • refusal to sign study consent form;
  • evidence or finding of another non-genetic cause of their condition;
  • Persons with known white matter disease or lesions related to: birth injury or prenatal injury, multiple sclerosis, trauma, infection, immunization, or post-infectious effects (e.g. ADEM- acute disseminated encephalomyelitis), metabolic disturbance (e.g. Central pontine myelinolysis), neoplasms, primary rheumatologic diseases (e.g. Systemic lupus erythematosis), stroke, hypoxic-ischemic injury, drug or toxin effect, seizures, or endocrine disturbance.

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Locations(1)

Primary Children's Hospital

Salt Lake City, Utah, United States

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NCT03639285


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