دورية أكاديمية

Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report

التفاصيل البيبلوغرافية
العنوان: Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report
المؤلفون: Katsuyuki Yokoi, Yoko Nakajima, Yuta Sudo, Tasuku Mariya, Rie Kawamura, Makiko Tsutsumi, Hidehito Inagaki, Tetsushi Yoshikawa, Tetsuya Ito, Hiroki Kurahashi
المصدر: JIMD Reports, Vol 63, Iss 6, Pp 575-580 (2022)
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
المجموعة: LCC:Diseases of the endocrine glands. Clinical endocrinology
LCC:Genetics
مصطلحات موضوعية: BCKDHA, FISH, maple syrup urine disease, paracentric inversion of Chromosome 19, whole‐exome sequencing, Diseases of the endocrine glands. Clinical endocrinology, RC648-665, Genetics, QH426-470
الوصف: Abstract Maple syrup urine disease (MSUD) is a rare autosomal recessive inherited disorder of branched‐chain amino acid metabolism caused by mutations in BCKDHA, BCKDHB, and DBT that encode the E1α, E1β, and E2 subunits of the branched‐chain α‐ketoacid dehydrogenase (BCKD) complex. Various MSUD‐causing variants have been described; however, no structural rearrangements in BCKDHA have been reported to cause the classic MSUD phenotype. Here, we describe the classic patient with MSUD with compound heterozygous pathogenic variants in BCKDHA: a missense variant (NM_000709.3:c.757G > A, NP_000700.1:p.Ala253Thr) and a paracentric inversion disrupting Intron 1 of BCKDHA, which was identified by whole‐genome sequencing and validated by fluorescence in situ hybridization. Using the sequence information of the breakpoint junction, we gained mechanistic insight into the development of this structural rearrangement. Furthermore, the establishment of junction‐specific polymerase chain reaction could facilitate identification of the variant in case carrier or future prenatal/preimplantation tests are necessary.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2192-8312
Relation: https://doaj.org/toc/2192-8312
DOI: 10.1002/jmd2.12333
URL الوصول: https://doaj.org/article/8e7589776bf14c6183443ec6dc96316b
رقم الأكسشن: edsdoj.8e7589776bf14c6183443ec6dc96316b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21928312
DOI:10.1002/jmd2.12333