G.O.7 Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency

Abstract Recently three different FLNC mutations were related to a peculiar phenotype of dominant distal myopathy with a distinct involvement of the hand muscles. Objective: We report the detailed clinical findings and underlying genetic defect in the Bulgarian family. Methods: We performed neurolog...

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Published in:	Neuromuscular disorders : NMD Vol. 22; no. 9; pp. 874 - 875
Main Authors:	Guergueltcheva, V, Peeters, K, Baets, J, Ceuterick-de Groote, C, Martin, J.J, Suls, A, Vriendt, E.D, Mihaylova, V, Chamova, T, Almeida-Souza, L, Ydens, E, Tzekov, C, Hadjidekov, G, Gospodinova, M, Storm, K, Reyniers, E, Bichev, S, van der Ven, P.F.M, Furst, D.O, Mitev, V, Lochmuller, H, Timmerman, V, Tournev, I, De Jonghe, P, Jordanova, A
Format:	Journal Article
Language:	English
Published:	Elsevier B.V 01-10-2012
Subjects:	Indexing in process Neurology
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Summary:	Abstract Recently three different FLNC mutations were related to a peculiar phenotype of dominant distal myopathy with a distinct involvement of the hand muscles. Objective: We report the detailed clinical findings and underlying genetic defect in the Bulgarian family. Methods: We performed neurological, electrophysiological, radiological and histopathological analyses of 13 patients and thirteen at-risk but asymptomatic individuals from three generations. Genome-wide parametric linkage analysis was followed by bidirectional sequencing of the filamin C (FLNC) gene. We characterized the identified nonsense mutation at cDNA and protein level. Results: Based on clinical findings, no known myopathy subtype was implicated in our distal myopathy patients. Light microscopic analysis of affected muscle tissue showed no specific hallmarks, however the electron microscopy revealed changes compatible with myofibrillar myopathy. Linkage studies delineated a 9.76 Mb region on chromosome 7q22.1-q35 containing filamin C ( FLNC ), a gene previously associated with myofibrillar myopathy. Mutation analysis revealed a novel c.5160delC frameshift deletion in all patients. The mutation results in a premature stop codon (p.Phe1720LeufsX63) that triggers nonsense-mediated mRNA decay. FLNC transcript levels were reduced in muscle and lymphoblast cells from affected subjects and partial loss of FLNC in muscle tissue was confirmed by protein analysis. Conclusions: The FLNC mutation that we identified is distinct in terms of the associated phenotype, muscle morphology and underlying molecular mechanism, thus extending the currently recognized clinical and genetic spectrum of filaminopathies. We conclude that filamin C is a dosage-sensitive gene and that FLNC haploinsufficiency can cause a specific type of myopathy in humans.
Bibliography:	ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23
ISSN:	0960-8966 1873-2364
DOI:	10.1016/j.nmd.2012.06.238