首页> 外文期刊>Neurological sciences >Frequency of familial aggregation in primary adult-onset cranial cervical dystonia.
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Frequency of familial aggregation in primary adult-onset cranial cervical dystonia.

机译:在成人成年发病的颅颈肌张力障碍中家族聚集的频率。

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摘要

Family history of definite/probable dystonia was studied in 36 probands with primary adult-onset cranial/cervical dystonia. Of the 157 relatives who were examined, 8 from 7 families and 11 from 10 families were diagnosed as having definite or probable dystonia, respectively. The frequency of familial occurrence of definite dystonia was 19.4%, 33% when considering both definite and probable dystonia. There was a tendency for relatives affected by either definite or probable dystonia to have the same type of dystonia as the index patient. Similar segregation ratios were found for parents, siblings, and children with either definite or probable dystonia. These observations raise the possibility that probable dystonia represents formes frustes/mild phenotypes of dystonia rather than another movement disorder.
机译:在36名先天性成年性颅/颈肌张力障碍的先证者中研究了确定/可能的肌张力障碍的家族史。在被检查的157个亲戚中,分别来自7个家庭的8个和来自10个家庭的11个被诊断为患有明确的或可能的肌张力障碍。家族性发生明确性肌张力障碍的频率为19.4%,同时考虑到明确性肌张力障碍和可能的肌张力障碍的发生率为33%。患有确定性或可能的肌张力障碍的亲属有与指数患者相同类型的肌张力障碍的趋势。父母,兄弟姐妹和患有确定性或可能性肌张力障碍的儿童的分离率相似。这些发现增加了可能的肌张力障碍代表肌张力障碍的轻度挫折/轻度表型而非另一种运动障碍的可能性。

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