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- W2005343416 abstract "We identified the first patient with infantile Refsum disease (IRD), a milder phenotype of peroxisome biogenesis disorder (PBD) caused by a mutated PEX3, and investigated the clinical, molecular and cellular characterization in this patient. The patient presented psychomotor regression, late-onset leukodystrophy, peripheral neuropathy, hearing impairment, a renal cyst, and renal hypertension and survived until the age of 36. Furthermore, fibroblasts from the patient indicated a mosaic pattern of catalase-positive particles (peroxisomes) and numerous peroxisomal membrane structures. Molecular analysis was homozygous for the D347Y mutation and reduced gene expression of PEX3 which encodes a peroxisomal membrane protein, pex3p, involved in peroxisome assembly at the early stage of peroxisomal membrane vesicle formation, therefore, patients with a mutated PEX3 gene have been reported to have only a severe phenotype of Zellweger syndrome and no or less peroxisomal remnant membrane structure. This is not only a newly identified milder PBD caused by a mutated PEX3 gene but also the first report of a Japanese patient with IRD who had not been diagnosed until over 30 years of age, which suggests there must be more variant PBD in patients with degenerative neurologic disorder, and to bring them to light is necessary." @default.
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- W2005343416 date "2013-10-01" @default.
- W2005343416 modified "2023-09-25" @default.
- W2005343416 title "Newly identified milder phenotype of peroxisome biogenesis disorder caused by mutated PEX3 gene" @default.
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- W2005343416 doi "https://doi.org/10.1016/j.braindev.2012.10.017" @default.
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