MedPath

Longitudinal Study of Neurodegenerative Disorders

Recruiting
Conditions
Vanishing White Matter Disease
Gaucher Disease
GAN
S-Adenosylhomocysteine Hydrolase Deficiency
Batten Disease
Tay-Sachs Disease
Lysosomal Storage Diseases
Multiple Sulfatase Deficiency Disease
Krabbe Disease
PKAN
Registration Number
NCT03333200
Lead Sponsor
University of Pittsburgh
Brief Summary

The purpose of this study is to understand the course of rare genetic disorders that affect the brain. This data is being analyzed to gain a better understanding of the progression of the rare neurodegenerative disorders and the effects of interventions.

Detailed Description

Patients would be evaluated by a multidisciplinary team at specific time points every 3 months the first year, every 6 months the second year and once a year thereafter.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1500
Inclusion Criteria
  • Any patient with a genetic neurodegenerative disorder
Exclusion Criteria
  • none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Language development15 years

Repeated standardized age equivalent scores.

Adaptive living skills15 years

Repeated standardized age equivalent scores.

Gross Motor development .15 years

Repeated standardized age equivalent scores.

Cognitive development15 years

Repeated standardized age equivalent scores.

Fine Motor development15 years

Repeated standardized age equivalent scores.

Secondary Outcome Measures
NameTimeMethod
Neurodegeneration of the brain as measured by MRI diffusion tensor imaging from birth to 5 years of age5 years

Specialized technique to use DTI data to measure brain degeneration over time

Exploratory biomarkers15 years

Blood, CSF and urine

Trial Locations

Locations (1)

UPMC Children's Hospital of Pittsburgh

🇺🇸

Pittsburgh, Pennsylvania, United States

© Copyright 2025. All Rights Reserved by MedPath