Clinical trials: RCDP2
Peroxisome Biogenesis Disorder, Zellweger Spectrum Disorder
Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)
The Peroxisome Biogenesis Disorders (PBD) are a group of inherited disorders due to defects in peroxisome assembly causing complex developmental and metabolic sequelae.
- Conditions
- Peroxisome Biogenesis Disorder, Zellweger Spectrum Disorder, RCDP - Rhizomelic Chondrodysplasia Punctata, D-Bifunctional Protein Deficiency
- Trial name
- NCT01668186
- Where
- Canada
- Volunteers
- 244 people
- Sponsor
- McGill University Health Centre/Research Institute of the McGill University Health Centre
RCDP - Rhizomelic Chondrodysplasia Punctata, RCDP1
Rhizomelic Chondrodysplasia Punctata Registry
The goal of this registry is to collect medical information on individuals with rhizomelic chondrodysplasia punctata and closely related conditions.
- Conditions
- RCDP - Rhizomelic Chondrodysplasia Punctata, RCDP1, RCDP2, RCDP3
- Trial name
- NCT04569162
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Nemours Children's Clinic