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- W4312067055 abstract "Abstract Ichthyosis follicularis with atrichia and photophobia (IFAP) syndrome is a rare genodermatosis characterized by a classic triad of follicular ichthyosis, alopecia, and photophobia. We report a Chinese patient displaying features of IFAP triad along with painful palmoplantar keratoderma, recurrent infections, periorificial keratotic plaques, nail dystrophy, and pachyonychia. Whole‐exome sequencing revealed an intronic variant (NM_015884.3: exon7:c.970+5G>A) in the gene MBTPS2 . Sanger sequencing confirmed that the variant segerated with phenotype in the family. Sequencing of cDNAs derived from the patient indicated the variant introduced a new splice donor site, leading to partial skipping of exon 7 (r.951_970del). An in vitro mini‐gene assay also revealed abnormal splicing of exon 7. This study presents a case complicated with X‐linked IFAP syndrome and Olmsted syndrome, and highlights the significance of using validation assays to identify the pathogenicity of intronic variants in MBTPS2 ." @default.
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- W4312067055 date "2022-12-20" @default.
- W4312067055 modified "2023-09-26" @default.
- W4312067055 title "An intronic splice‐site variant in <i>MBTPS2</i> underlies ichthyosis follicularis with atrichia and photophobia syndrome" @default.
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- W4312067055 doi "https://doi.org/10.1111/1346-8138.16684" @default.
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