SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Salari H)
 

Search: WFRF:(Salari H) > Ataxia-telangiectas...

  • Sedghi, M. (author)

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • 2018-12-03
  • Ovid Technologies (Wolters Kluwer Health),2018

Numbers

  • LIBRIS-ID:oai:gup.ub.gu.se/277527
  • https://gup.ub.gu.se/publication/277527URI
  • https://doi.org/10.1212/nxg.0000000000000295DOI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Objective We report 3 siblings with the characteristic features of ataxia-telangiectasia-like disorder associated with a homozygous MREll synonymous variant causing nonsense-mediated mRNA decay (NMD) and MRE11A deficiency. Clinical assessments, next-generation sequencing, transcript and immunohistochemistry analyses were performed. The patients presented with poor balance, developmental delay during the first year of age, and suffered from intellectual disability from early childhood. They showed oculomotor apraxia, slurred and explosive speech, limb and gait ataxia, exaggerated deep tendon reflex, dystonic posture, and mirror movement in their hands. They developed mild cognitive abilities. Brain MRI in the index case revealed cerebellar atrophy. Next-generation sequencing revealed a homozygous synonymous variant in MRE11 (c.657C>T, p.Asn219=) that we show affects splicing. A complete absence of MREll transcripts in the index case suggested NMD and immunohistochemistry confirmed the absence of a stable protein. Despite the critical role of MRE11A in double-strand break repair and its contribution to the Mre11/Rad50/Nbs1 complex, the absence of MRE11A is compatible with life.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Salari, M. (author)
  • Moslemi, Ali-RezaGothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology(Swepub:gu)xmosal (author)
  • Kariminejad, A. (author)
  • Davis, M. (author)
  • Goullee, H. (author)
  • Olsson, B. (author)
  • Laing, N. (author)
  • Tajsharghi, H. (author)
  • Göteborgs universitetInstitutionen för biomedicin, avdelningen för patologi (creator_code:org_t)

Related titles

  • In:Neurology-Genetics: Ovid Technologies (Wolters Kluwer Health)4:62376-7839

Internet link

Find in a library

To the university's database

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view