Disorders of Cerebral Development: A Phenotypic and Genetic Analysis

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Dr. Elliott Sherr and his collaborators at University of California, San Francisco (UCSF) are studying the genetic causes of disorders of cognition and epilepsy, in particular disorders of brain development that affect the corpus callosum, such as Aicardi syndrome, as well as two additional brain malformations, polymicrogyria and Dandy-Walker malformation. The goal of the investigators' research is to use a better understanding of the underlying genetic causes as a foundation to develop better treatments for these groups of patients.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Clinical diagnosis of agenesis or dysgenesis of the corpus callosum, polymicrogyria, or Dandy-Walker malformation

• Should be confirmed by an MRI (Magnetic Resonance Imaging) of the brain

Locations
United States
California
University of California, San francisco
RECRUITING
San Francisco
Contact Information
Primary
Carolyn Le, BA, BS
Carolyn.Le@ucsf.edu
415-502-8039
Time Frame
Start Date: 2003-08
Estimated Completion Date: 2025-01
Participants
Target number of participants: 2000
Sponsors
Leads: University of California, San Francisco
Collaborators: University of Washington, California Institute of Technology

This content was sourced from clinicaltrials.gov

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