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Sökning: WFRF:(Oldfors Anders 1951) > (2005-2009) > A mutation in the f...

A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis

Kimber, Eva, 1951 (författare)
Uppsala universitet,Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Institutionen för kvinnors och barns hälsa,Barnneurologisk forskning/Ahlsten,Department of Neuropediatrics, Uppsala University Children's Hospital, Uppsala, Sweden /
Tajsharghi, Homa, 1968 (författare)
Department of Pathology, Sahlgrenska University Hospital, Sweden
Kroksmark, Anna-Karin (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Queen Silvia Children's Hospital, Sahlgrenska Academy, University of Göteborg, Göteborg, Sweden
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Oldfors, Anders, 1951 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för patologi,Institute of Biomedicine, Department of Pathology,Department of Pathology, Sahlgrenska University Hospital, Sweden
Tulinius, Mar, 1953 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences,Queen Silvia Children's Hospital, Sahlgrenska Academy, University of Göteborg, Göteborg, Sweden
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 (creator_code:org_t)
Ovid Technologies (Wolters Kluwer Health), 2006
2006
Engelska.
Ingår i: Neurology. - : Ovid Technologies (Wolters Kluwer Health). - 1526-632X .- 0028-3878. ; 67:4, s. 597-601
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVE: To describe a three-generation family with distal arthrogryposis associated with myopathy and caused by a mutation in the gene encoding for sarcomeric thin filament protein troponin I, TNNI2. METHODS: The authors performed clinical investigations and reviewed medical records. Muscle biopsy specimens were obtained for morphologic analysis. Genomic DNA was extracted from blood and analyzed for mutations in TNNI2. RESULTS: The five affected individuals had predominantly distal congenital joint contractures, mild facial involvement (mild micrognathia, narrow palpebral fissures), and no detectable muscle weakness. The four affected adults had slightly increased levels of creatine kinase in blood, and muscle biopsy specimens showed findings of myopathy with changes restricted to type 2 fibers. These included variability of muscle fiber size, internalized nuclei, and increased interstitial connective tissue. Analysis of TNNI2 encoding the troponin I isoform expressed in type 2 muscle fibers disclosed a heterozygous three-base in-frame deletion, 2,918-2,920del, skipping the highly conserved lysine at position 176. The mutation was present in all 5 affected individuals but was not identified in any of the 11 unaffected family members. CONCLUSION: Distal arthrogryposis type 1 is genetically heterogeneous, and myopathy due to sarcomeric protein dysfunction may be one underlying cause of the disease.

Ämnesord

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

Nyckelord

Adult
Arthrogryposis/*epidemiology/*genetics
DNA Mutational Analysis
Distal Myopathies/*epidemiology/*genetics
Female
Genetic Predisposition to Disease/epidemiology/genetics
Humans
Male
Muscle Fibers
Fast-Twitch/*metabolism
Muscle
Skeletal/*metabolism
Mutation
Pedigree
Protein Isoforms/genetics
Risk Assessment/methods
Risk Factors
Sweden/epidemiology
Troponin I/*genetics
MEDICINE
Medical sciences

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