Academic Journal
A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination
| العنوان: | A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination |
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| المؤلفون: | Miyamoto, Sachiko, Nakashima, Mitsuko, Ohashi, Tsukasa, Hiraide, Takuya, Kurosawa, Kenji, Yamamoto, Toshiyuki, Takanashi, Junichi, Osaka, Hitoshi, Inoue, Ken, Miyazaki, Takehiro, Wada, Yoshinao, Okamoto, Nobuhiko, Saitsu, Hirotomo |
| المساهمون: | Japan Society for the Promotion of Science, Japan Agency for Medical Research and Development, Ministry of Health, Labour and Welfare, Takeda Science Foundation |
| المصدر: | Molecular Genetics & Genomic Medicine ; volume 7, issue 8 ; ISSN 2324-9269 2324-9269 |
| بيانات النشر: | Wiley |
| سنة النشر: | 2019 |
| المجموعة: | Wiley Online Library (Open Access Articles via Crossref) |
| الوصف: | Background Congenital disorders of glycosylation (CDGs) are genetic diseases caused by pathogenic variants of genes involved in protein or lipid glycosylation. De novo variants in the SLC35A2 gene, which encodes a UDP‐galactose transporter, are responsible for CDGs with an X‐linked dominant manner. Common symptoms related to SLC35A2 variants include epilepsy, psychomotor developmental delay, hypotonia, abnormal facial and skeletal features, and various magnetic resonance imaging (MRI) findings. Methods Whole‐exome sequencing was performed on the patient's DNA, and candidate variants were confirmed by Sanger sequencing. cDNA analysis was performed to assess the effect of the splice site variant using peripheral leukocytes. The X‐chromosome inactivation pattern was studied using the human androgen receptor assay. Results We identified a de novo splice site variant in SLC35A2 (NM_005660.2: c.274+1G>A) in a female patient who showed severe developmental delay, spastic paraplegia, mild cerebral atrophy, and delayed myelination on MRI, but no seizures. The variant led to an aberrant splicing resulting in an in‐frame 33‐bp insertion, which caused an 11‐amino acid insertion in the presumptive cytoplasmic loop. X‐inactivation pattern was random. Partial loss of galactose and sialic acid of the N ‐linked glycans of serum transferrin was observed. Conclusion This case would expand the phenotypic spectrum of SLC35A2 ‐related disorders to delayed myelination with spasticity and no seizures. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1002/mgg3.814 |
| الاتاحة: | http://dx.doi.org/10.1002/mgg3.814 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmgg3.814 https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.814 https://onlinelibrary.wiley.com/doi/full-xml/10.1002/mgg3.814 https://onlinelibrary.wiley.com/doi/am-pdf/10.1002%2Fmgg3.814 |
| Rights: | http://creativecommons.org/licenses/by/4.0/ |
| رقم الانضمام: | edsbas.355889AC |
| قاعدة البيانات: | BASE |
| DOI: | 10.1002/mgg3.814 |
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