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ArtikelDiagnosis and etiology of congenital muscular dystrophy  
Oleh: Peat, R. A. ; Smith, J. M. ; Compton, A. G. ; Baker, N. L. ; Pace, R. A.
Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 05 (Jul. 2008), page 312-321.
Topik: CREATINE KINASE; ELECTROMYOGRAM; WALKER-WARBURG SYNDROME
Ketersediaan
  • Perpustakaan FK
    • Nomor Panggil: N11.K.2008.01
    • Non-tandon: 1 (dapat dipinjam: 0)
    • Tandon: tidak ada
    Lihat Detail Induk
Isi artikelObjective: We aimed to determine the frequency of all known forms of congenital muscular dystrophy (CMD) in a large Australasian cohort. Methods: We screened 101 patients with CMD with a combination of immunofluorescence, Western blotting, and DNA sequencing to identify disease-associated abnormalities in glycosylated {alpha}-dystroglycan, collagen VI, laminin {alpha}2, {alpha}7-integrin, and selenoprotein. Results: A total of 45% of the CMD cohort were assigned to an immunofluorescent subgroup based on their abnormal staining pattern. Abnormal staining for glycosylated {alpha}-dystroglycan was present in 25% of patients, and approximately half of these had reduced glycosylated {alpha}-dystroglycan by Western blot. Sequencing of the FKRP, fukutin, POMGnT1, and POMT1 genes in all patients with abnormal {alpha}-dystroglycan immunofluorescence identified mutations in one patient for each of these genes and two patients had mutations in POMT2. Twelve percent of patients had abnormalities in collagen VI immunofluorescence, and we identified disease-causing COL6 mutations in eight of nine patients in whom the genes were sequenced. Laminin {alpha}2 deficiency accounted for only 8% of CMD. {alpha}7-Integrin staining was absent in 12 of 45 patients studied, and ITGA7 gene mutations were excluded in all of these patients. Conclusions: We define the distribution of different forms of congenital muscular dystrophy in a large cohort of mixed ethnicity and demonstrate the utility and limitations of current diagnostic techniques.
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