Inherited myoclonus dystonia (M-D, DYTH) is an autosomal dominant dystonia-plus syndrome, which in many families is caused by mutations in the SGCE/tepsilon-sarcoglycan gene. We present a family with M-D, with an unusual presentaion characterized by infantile onset with falls in two sisters and adult-onset writer's cramp in their father. Myoclonus dystonia is typically characterized by a variable mixture of alcohol-sensitive myoclonie jerks and dystonia classically affecting mainly the proximal arms and neck. Leg involvement is less frequent, and to our knowledge, initial presentation with falls has not previously been described. The unusual phenotype of the family is discussed. (C) 2008 Movement Disorder Society

Unusual Familial Presentation of Epsilon-Sarcoglycan Gene Mutation with Falls and Writer's Cramp

VALENTE, ENZA MARIA;
2008-01-01

Abstract

Inherited myoclonus dystonia (M-D, DYTH) is an autosomal dominant dystonia-plus syndrome, which in many families is caused by mutations in the SGCE/tepsilon-sarcoglycan gene. We present a family with M-D, with an unusual presentaion characterized by infantile onset with falls in two sisters and adult-onset writer's cramp in their father. Myoclonus dystonia is typically characterized by a variable mixture of alcohol-sensitive myoclonie jerks and dystonia classically affecting mainly the proximal arms and neck. Leg involvement is less frequent, and to our knowledge, initial presentation with falls has not previously been described. The unusual phenotype of the family is discussed. (C) 2008 Movement Disorder Society
2008
Molecular Biology & Genetics considers all aspects of basic and applied genetics, including molecular genetics, prokaryotic and eukaryotic gene expression, mechanisms of mutagenesis, structure, function and regulation of genetic material. Also included are resources concerned with clinical genetics, patterns of inheritance, genetic cause, and screening and treatment of disease. Resources dealing specifically with developmentally regulated gene expression, or with signal transduction pathways that modulate gene expression at the cellular level are excluded and are covered in the Cell and Developmental Biology category.
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Esperti anonimi
Inglese
Internazionale
23
13
1913
1915
3
5
info:eu-repo/semantics/article
262
Koukouni, Vasiliki; Valente, ENZA MARIA; Cordivari, Carla; Bhatia, Kailash P.; Quinn, Niall P.
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1180538
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