Recurrent Ischemic Strokes due to Monogenic COL4A1 Mutation: The First Case Report from Latin America.

Emilio Israel Wong-Valenzuela, Daniel San Juan, José Santos Zambrano, Alejandra Camacho Molina, Miguel Angel Morales-Morales, Alejandro Lopez-Landa
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Abstract

Introduction. Monogenic mutations as the cause of recurrent ischemic cerebral small-vessel disease with leukodystrophy are rare. COL4A1 gene mutations are a relatively new etiology of cerebrovascular lesions in young adults; however, any patient has been reported from Latin America. Case Presentation. We presented a Mexican young female with leukodystrophy and recurrent stroke secondary to COL4A1 monogenic mutation. Discussion/Conclusion. COL4A1 monogenic mutations are associated with cerebral small-vessel disease and other systemic manifestations. To date, there is little evidence to justify the treatment and prevention of recurrent strokes in patients with this mutation.

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单基因COL4A1突变引起的缺血性卒中复发:拉丁美洲首例报告。
介绍。单基因突变是复发性缺血性脑血管病伴脑白质营养不良的罕见病因。COL4A1基因突变是年轻人脑血管病变的一个相对较新的病因;然而,拉丁美洲报告了任何患者。案例演示。我们提出了一个墨西哥年轻女性脑白质营养不良和复发性中风继发于COL4A1单基因突变。讨论和结论。COL4A1单基因突变与脑小血管疾病和其他系统性表现有关。迄今为止,几乎没有证据证明治疗和预防这种突变患者的复发性中风是合理的。
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