Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

被引:24
作者
Meuleman, J
Kuhlenbäumer, G
Schirmacher, A
Wehnert, M
De Jonghe, P
De Vriendt, E
Young, P
Airaksinen, E
Pou-Serradell, A
Prats, JM
Ringelstein, B
Stögbauer, F
Van Broeckhoven, C
Timmerman, V
机构
[1] Univ Antwerp, Dept Biochem, Genet Mol Lab, Peripheral Neuropathy Grp, B-2610 Antwerp, Belgium
[2] Univ Antwerp VIB, Dept Biochem, Born Bunge Fdn, Dept Mol Genet, B-2610 Antwerp, Belgium
[3] Univ Hosp Munster, Dept Neurol, Munster, Germany
[4] Ernst Moritz Arndt Univ Greifswald, Inst Human Genet, Greifswald, Germany
[5] Univ Antwerp Hosp, Div Neurol, Antwerp, Belgium
[6] Univ Barcelona, Dept Neurol, Barcelona, Spain
[7] Hosp Cruces, Dept Pediat, Baracaldo, Spain
关键词
hereditary neuralgic amyotrophy; molecular genetics; linkage analysis;
D O I
10.1038/sj.ejhg.5200384
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant, recurrent focal neuropathy. HNA is characterised by episodes of painful brachial plexus neuropathy with muscle weakness and atrophy, as well as sensory disturbances. Single episodes are commonly preceded by non-specific infections, immunisations or parturition. Mild dysmorphic features and short stature are present in some HNA families, but absolute co-segregation with HNA has not been described. To refine the previously described HNA locus on chromosome 17q25, we performed a genetic linkage study in five HNA families with different geographic origins. Significant linkage was obtained with chromosome 17q24-q25 short tandem repeat (STR) markers in three HNA families and suggestive linkage was found in the other two HNA families. Analysis of the informative recombinations in affected individuals allowed us to reduce the HNA linkage interval to a candidate region of 3.5 cM.
引用
收藏
页码:920 / 927
页数:8
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