Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)

Clinical trial NCT01668186 · RECRUITING

Trial details

NCT number: NCT01668186
Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre
Status: RECRUITING
Study type: OBSERVATIONAL

Peroxisome Biogenesis Disorder Zellweger Spectrum Disorder RCDP - Rhizomelic Chondrodysplasia Punctata D-Bifunctional Protein Deficiency Alpha-Methylacyl-CoA Racemase Deficiency Peroxisomal Acyl-CoA Oxidase Deficiency Peroxisomal Acyl-CoA Oxidase 2 Deficiency ATP Binding Cassette Subfamily D Member 3 Gene Mutation ACBD5 (AcylCoA Binding Domain 5) Deficiency Adult Refsum Disease Sterol Carrier Protein 2 Deficiency

Start date: 2012-01-01
Primary completion: 2030-01-01
Enrollment: 244

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