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Updated: Jul 16, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Phenotype of adult Refsum disease due to a defect in peroxin 7
M A Horn1, D M van den Brink, R J A Wanders
1Department of Neurology, Ulleval University Hospital, Oslo, Norway. rtho@uus.no
Abstract:
The biochemical hallmark of adult Refsum disease (ARD) is an isolated deficiency in the breakdown of phytanic acid. This usually results from a PHYH gene defect, although some cases have been found to carry a PEX7 defect. We describe the phenotype of such a patient, indistinguishable from that of classic ARD. Hence, we propose the subdivision of ARD into type 1 and type 2, depending on which gene is defective.
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