SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Quinlivan Rosaline)
 

Search: WFRF:(Quinlivan Rosaline) > Hereditary myopathy...

Hereditary myopathy with early respiratory failure: occurrence in various populations

Palmio, Johanna (author)
Evila, Anni (author)
Chapon, Francoise (author)
show more...
Tasca, Giorgio (author)
Xiang, Fengqing (author)
Karolinska Institutet
Brådvik, Björn (author)
Lund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine
Eymard, Bruno (author)
Echaniz-Laguna, Andoni (author)
Laporte, Jocelyn (author)
Karppa, Mikko (author)
Mahjneh, Ibrahim (author)
Quinlivan, Rosaline (author)
Laforet, Pascal (author)
Damian, Maxwell (author)
Berardo, Andres (author)
Taratuto, Ana Lia (author)
Bueri, Jose Antonio (author)
Tommiska, Johanna (author)
Raivio, Taneli (author)
Tuerk, Matthias (author)
Goelitz, Philipp (author)
Chevessier, Frederic (author)
Sewry, Caroline (author)
Norwood, Fiona (author)
Hedberg, Carola, 1969 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology
Schroeder, Rolf (author)
Edstrom, Lars (author)
Oldfors, Anders, 1951 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology
Hackman, Peter (author)
Udd, Bjarne (author)
show less...
 (creator_code:org_t)
2013-04-19
2014
English.
In: Journal of Neurology, Neurosurgery and Psychiatry. - : BMJ. - 1468-330X .- 0022-3050. ; 85:3, s. 345-353
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Objective Several families with characteristic features of hereditary myopathy with early respiratory failure (HMERF) have remained without genetic cause. This international study was initiated to clarify epidemiology and the genetic underlying cause in these families, and to characterise the phenotype in our large cohort. Methods DNA samples of all currently known families with HMERF without molecular genetic cause were obtained from 12 families in seven different countries. Clinical, histopathological and muscle imaging data were collected and five biopsy samples made available for further immunohistochemical studies. Genotyping, exome sequencing and Sanger sequencing were used to identify and confirm sequence variations. Results All patients with clinical diagnosis of HMERF were genetically solved by five different titin mutations identified. One mutation has been reported while four are novel, all located exclusively in the FN3 119 domain (A150) of A-band titin. One of the new mutations showed semirecessive inheritance pattern with subclinical myopathy in the heterozygous parents. Typical clinical features were respiratory failure at mid-adulthood in an ambulant patient with very variable degree of muscle weakness. Cytoplasmic bodies were retrospectively observed in all muscle biopsy samples and these were reactive for myofibrillar proteins but not for titin. Conclusions We report an extensive collection of families with HMERF with five different mutations in exon 343 of TTN, which establishes this exon as the primary target for molecular diagnosis of HMERF. Our relatively large number of new families and mutations directly implies that HMERF is not extremely rare, not restricted to Northern Europe and should be considered in undetermined myogenic respiratory failure.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

EPIDEMIOLOGY
GENETICS
MYOPATHY

Publication and Content Type

art (subject category)
ref (subject category)

Find in a library

To the university's database

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