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伴动眼性失用症2型共济失调的频率和表型谱:18例患者的临床和遗传学研究

Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.

作者信息

Le Ber Isabelle, Bouslam Naïma, Rivaud-Péchoux Sophie, Guimarães João, Benomar Ali, Chamayou Céline, Goizet Cyril, Moreira Maria-Ceù, Klur Sandra, Yahyaoui Mohamed, Agid Yves, Koenig Michel, Stevanin Giovanni, Brice Alexis, Dürr Alexandra

机构信息

Fédération de Neurologie, Hôpital Pitié-Salpêtrière AP-HP, Paris, France.

出版信息

Brain. 2004 Apr;127(Pt 4):759-67. doi: 10.1093/brain/awh080. Epub 2004 Jan 21.

Abstract

Ataxia with oculomotor apraxia type 2 (AOA2) is a newly described autosomal recessive cerebellar ataxia (ARCA) defined by genetic location to 9q34 of three families sharing gait ataxia, oculomotor apraxia and/or elevated alpha-foetoprotein (AFP) levels. We have evaluated 77 families with progressive non-Friedreich ARCA and have identified six families with a phenotype suggestive of AOA2. Linkage was confirmed in all six families, with a maximal lod score of 5.91 at D9S1830. We report the first detailed phenotypic study, including neuropsychological, oculographic and brain imaging investigations, in the largest series of AOA2 patients yet recruited. The mean age at onset was 15.1 +/- 3.8 years. Sensory motor neuropathy (92%) and choreic or dystonic movements (44%) were frequent. Oculomotor apraxia was observed in 56% of patients and characterized by increased horizontal saccade latencies and hypometria. AFP levels were elevated in 100% of the families, making it a useful biological marker. This study shows for the first time that AOA2 can be found in Europe, North Africa and the West Indies, and its relative frequency represents approximately 8% of non-Friedreich ARCA, which is more frequent than ataxia telangiectasia and ataxia with oculomotor apraxia type 1 (AOA1), in our series of adult patients. In adults, AOA2 may be, therefore, the most frequent cause of ARCA identified so far, after Friedreich's ataxia.

摘要

2型动眼性失用型共济失调(AOA2)是一种新描述的常染色体隐性小脑共济失调(ARCA),其依据是三个患有步态共济失调、动眼性失用和/或甲胎蛋白(AFP)水平升高的家族在基因上定位于9q34。我们评估了77个患有进行性非弗里德赖希型ARCA的家族,并鉴定出6个具有提示AOA2表型的家族。在所有6个家族中均证实存在连锁关系,在D9S1830处的最大对数计分高达5.91。我们报告了在迄今招募的最大系列AOA2患者中进行的首次详细表型研究,包括神经心理学、眼动图和脑成像检查。发病的平均年龄为15.1±3.8岁。感觉运动神经病(92%)和舞蹈样或张力障碍性运动(44%)很常见。56%的患者观察到动眼性失用,其特征为水平扫视潜伏期延长和幅度减小。100%的家族中AFP水平升高,使其成为一种有用的生物学标志物。这项研究首次表明,AOA2在欧洲、北非和西印度群岛均有发现,在我们的成年患者系列中,其相对频率约占非弗里德赖希型ARCA的8%,比共济失调毛细血管扩张症和1型动眼性失用型共济失调(AOA1)更为常见。因此,在成年人中,AOA2可能是迄今确定的继弗里德赖希共济失调之后最常见的ARCA病因。

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