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New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations
Department of Pathology, Sahlgrenska University Hospital, Göteborg, Sweden.
AP-HP, Service de Pédiatrie, Centre National de Référence des Maladies Neuromusculaires GNMH, Garches, France.
Department of Pediatrics, Sahlgrenska University Hospital, Göteborg, Sweden.
Institut de Myologie, Groupe Hospitalier Pitie-Salpêtrière, Paris, France.
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2008 (English)In: Neurology, ISSN 0028-3878, E-ISSN 1526-632X, Vol. 71, no 23, 1896-1901 p.Article in journal (Refereed) Published
Abstract [en]

OBJECTIVE: Mutations in the beta-tropomyosin gene (TPM2) are a rare cause of congenital myopathies with features of nemaline myopathy and cap disease and may also cause distal arthrogryposis syndromes without major muscle pathology. We describe the muscle biopsy findings in three patients with cap disease and novel heterozygous mutations in TPM2.

METHODS: Three unrelated patients with congenital myopathy were investigated by muscle biopsy and genetic analysis.

RESULTS: All three patients had early-onset muscle weakness of variable severity and distribution. Muscle biopsy demonstrated in all three patients near uniformity of type 1 fibers and an unusual irregular and coarse-meshed intermyofibrillar network. By electron microscopy, the myofibrils were broad and partly split, and the Z lines appeared jagged. In one of the patients caps structures were identified only by electron microscopy, and in one patient they were identified only in a second biopsy at adulthood. Three novel, de novo, heterozygous mutations in TPM2 were identified: a three-base pair deletion in-frame (p.Lys49del), a three-base pair duplication in-frame (p.Gly52dup), and a missense mutation (p.Asn202Lys).

CONCLUSIONS: Mutations in TPM2 seem to be a frequent cause of cap disease. Because cap structures may be sparse, other prominent features, such as a coarse-meshed intermyofibrillar network and jagged Z lines, may be clues to correct diagnosis and also indicate that the pathogenesis involves defective assembly of myofilaments.

Place, publisher, year, edition, pages
American Academy of Neurology , 2008. Vol. 71, no 23, 1896-1901 p.
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Research subject
Medical sciences
URN: urn:nbn:se:his:diva-11962DOI: 10.1212/01.wnl.0000336654.44814.b8ISI: 000261268000012PubMedID: 19047562ScopusID: 2-s2.0-63849099977OAI: oai:DiVA.org:his-11962DiVA: diva2:906959
Available from: 2016-02-25 Created: 2016-02-25 Last updated: 2016-03-04Bibliographically approved

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