Browse

Explore conditions, clinical trials, and the organisations running them.

Up to: Developmental anomaly of metabolic origin · Peroxisome biogenesis disorder

Zellweger spectrum disorders

The most severe variant seen in the peroxisome biogenesis disorders that is characterized by neuronal migration defects in the brain, dysmorphic craniofacial features, profound hypotonia, neonatal seizures, and liver dysfunction.

6 trials tagged with this condition →

Peroxisome biogenesis disorder due to PEX1 defect 0 trials · 1 incl. sub-types Sub-types →
Peroxisome biogenesis disorder 9B 0 trials
Peroxisome biogenesis disorder due to PEX10 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX11B defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX12 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX13 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX14 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX16 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX19 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX2 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX26 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX3 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX5 defect 0 trials Sub-types →
Peroxisome biogenesis disorder due to PEX6 defect 0 trials Sub-types →
Peroxisome biogenesis disorder, complementation group 2 0 trials