Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants
| العنوان: | Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants |
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| المؤلفون: | Moeenaldeen Al-Sayed, Yin-Hsiu Chien, Francesca D’Avanzo, Rodolfo Tonin, Hsiang-Yu Lin, Akashdeep Singh, Emanuela Izzo, Ana Carolina Brusius-Facchin, Alessandra Zanetti, Laura Pollard, David C Kasper, Roberto Giugliani, Shuan-Pei Lin, Rosella Tomanin, Tim Wood, Amelia Morrone |
| المصدر: | Human Mutation. 42:1384-1398 |
| بيانات النشر: | Hindawi Limited, 2021. |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | Genetics, Newborn screening, Genetic counseling, Mucopolysaccharidosis, Mucopolysaccharidosis IV, Biology, Compound heterozygosity, medicine.disease, Chondroitinsulfatases, Frameshift mutation, Mutation, medicine, Humans, Missense mutation, Allele, Gene, Genetic Association Studies, Genetics (clinical) |
| الوصف: | Mucopolysaccharidosis IVA (MPS IVA, Morquio A syndrome) is a rare autosomal recessive lysosomal storage disorder caused by mutations in the N-acetylgalactosamine-6-sulfatase (GALNS) gene. We collected, analyzed, and uniformly summarized all published GALNS gene variants, thus updating the previous mutation review by Morrone, et al. 2014. In addition, new variants were communicated by seven reference laboratories in Europe, the Middle East, Latin America, Asia, and the USA. All data were analyzed to determine common alleles, geographic distribution, level of homozygosity, and genotype-phenotype correlation. Moreover, variants were classified according to their pathogenicity as suggested by ACMG. Including those previously published, we assembled 446 unique variants, among which 68 were novel, from 1190 subjects (including newborn screening positive subjects). Variants distribution was missense (65.0%), followed by nonsense (8.1%), splicing (7.2%), small frameshift deletions(del)/insertions(ins) (7.0%), intronic (4.0%), and large del/ins and complex rearrangements (3.8%). Half (50.4%) of the subjects were homozygous, 37.1% were compound heterozygous, and 10.7% had only one variant detected. The novel variants underwent in silico analysis to evaluate their pathogenicity. All variants were submitted to ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) to make them publicly available. Mutation updates are essential for the correct molecular diagnoses, genetic counselling, prenatal and preimplantation diagnosis, and disease management. This article is protected by copyright. All rights reserved. |
| تدمد: | 1098-1004 1059-7794 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb41b8131b26c8b3f9f3a3fa629b7906 https://doi.org/10.1002/humu.24270 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....bb41b8131b26c8b3f9f3a3fa629b7906 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 10981004 10597794 |
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