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Emery-Dreifuss muscular dystrophy: a novel mutation in the LMNA gene

P. Laššuthová, L. Baránková, J. Kraus, T. Maříková, P. Seeman

. 2009 ; 41 (2) : 127-130.

Language English Country United States

Document type Case Reports, Research Support, Non-U.S. Gov't

Persistent link   https://www.medvik.cz/link/bmc11016746

Described here is the phenotypical expression of a novel LMNA mutation c.1157 G>T in a Czech patient with an early-onset form of Emery-Dreifuss muscular dystrophy. The mutation predicts aberrant splicing. Now 21 years old, the patient has had slowly progressing muscle dystrophy since the age of one and early contractures of elbows. He is the only family member affected. Even though the dystrophy typically affects the heart as well, in the present case these signs are not yet expressed.

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$a Department of Child Neurology, Second School of Medicine, Charles University Prague, Prague, Czech Republic. petra.lassuthova@gmail.com
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$a Described here is the phenotypical expression of a novel LMNA mutation c.1157 G>T in a Czech patient with an early-onset form of Emery-Dreifuss muscular dystrophy. The mutation predicts aberrant splicing. Now 21 years old, the patient has had slowly progressing muscle dystrophy since the age of one and early contractures of elbows. He is the only family member affected. Even though the dystrophy typically affects the heart as well, in the present case these signs are not yet expressed.
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