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部分性癫痫与47,XXX核型:4例报告

Partial epilepsy and 47,XXX karyotype: report of four cases.

作者信息

Roubertie Agathe, Humbertclaude Véronique, Leydet Julie, Lefort Geneviève, Echenne Bernard

机构信息

Service de Neuropédiatrie, Hôpital Gui de Chauliac, Montpellier, France.

出版信息

Pediatr Neurol. 2006 Jul;35(1):69-74. doi: 10.1016/j.pediatrneurol.2006.01.003.

Abstract

Epilepsy is a common finding in chromosomal imbalances, but only a few chromosome abnormalities have a characteristic electro-clinical pattern. Trisomy X is one of the most common sex chromosome abnormalities in females, and is associated with considerable phenotypic variability. This report describes four 47,XXX females with mental deficiency and epilepsy. Although a specific electro-clinical pattern could not be defined, the epileptic phenotypes of these patients share many features; we suggest that the association 47,XXX/epilepsy/mental retardation may not be coincidental. This report also enlarges the clinical spectrum of the 47,XXX phenotype. Moreover, these observations highlight the critical role of chromosome X in epilepsy and mental retardation.

摘要

癫痫是染色体失衡中的常见表现,但只有少数染色体异常具有特征性的电临床模式。X三体综合征是女性中最常见的性染色体异常之一,与相当大的表型变异性相关。本报告描述了四名患有智力缺陷和癫痫的47,XXX女性。虽然无法确定特定的电临床模式,但这些患者的癫痫表型有许多共同特征;我们认为47,XXX/癫痫/智力迟钝之间的关联可能并非偶然。本报告还扩大了47,XXX表型的临床谱。此外,这些观察结果突出了X染色体在癫痫和智力迟钝中的关键作用。

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