Zellweger spectrum disorders
MONDO:0019609The 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.
Also known as: ZS, ZWS, Zellweger spectrum disorders, Zellweger syndrome, cerebrohepatorenal syndrome, Zellweger leukodystrophy
15 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Peroxisome biogenesis disorder 1B
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Peroxisome biogenesis disorder 10A (Zellweger)
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Peroxisome biogenesis disorder 10B
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Peroxisome biogenesis disorder 11A (Zellweger)
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Peroxisome biogenesis disorder 11B
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Peroxisome biogenesis disorder 12A (Zellweger)
(0)
Peroxisome biogenesis disorder 13A (Zellweger)
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Peroxisome biogenesis disorder 14B
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Peroxisome biogenesis disorder 1A (Zellweger)
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Peroxisome biogenesis disorder 2A (Zellweger)
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Peroxisome biogenesis disorder 2B
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Peroxisome biogenesis disorder 3A (Zellweger)
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Peroxisome biogenesis disorder 4A (Zellweger)
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Peroxisome biogenesis disorder 4B
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Peroxisome biogenesis disorder 5A (Zellweger)
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Peroxisome biogenesis disorder 5B
(0)
Peroxisome biogenesis disorder 6A (Zellweger)
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Peroxisome biogenesis disorder 6B
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Peroxisome biogenesis disorder 7A (Zellweger)
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Peroxisome biogenesis disorder 7B
(0)