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中风的孟德尔病因。

Mendelian etiologies of stroke.

作者信息

Natowicz M, Kelley R I

机构信息

Division of Genetics, Children's Hospital of Philadelphia, PA 19104.

出版信息

Ann Neurol. 1987 Aug;22(2):175-92. doi: 10.1002/ana.410220202.

Abstract

There are many genetic disorders associated with an increased risk for stroke that may easily be overlooked in the evaluation of both adult and pediatric acute stroke victims. The recognition of a genetic disorder as the cause of a stroke has important implications not only for the immediate care of the stroke victim, but often also for others in the patient's family who may be at risk for the same disease and for whom preventive measures sometimes can be taken. We present here a comprehensive review of genetic disorders associated with stroke in the nongeriatric age groups for which a causative role in the evolution of stroke has been recognized or is likely. For each disorder, the major clinical and biochemical characteristics as well as the probable pathogenetic mechanisms of stroke are discussed, together with the appropriate testing required to screen for and confirm the diagnosis. The great variety of genetic disorders and mechanisms causing stroke underscores the increasing importance of understanding genetic disease for appropriate diagnosis and treatment of a common clinical problem affecting both children and adults.

摘要

有许多与中风风险增加相关的遗传疾病,在评估成人和儿童急性中风患者时很容易被忽视。识别遗传疾病是中风的病因不仅对中风患者的即时护理具有重要意义,而且通常对患者家族中其他可能有患同一种疾病风险且有时可采取预防措施的人也很重要。我们在此全面综述非老年年龄组中与中风相关的遗传疾病,这些疾病在中风的发生发展中已被确认为具有致病作用或可能具有致病作用。对于每种疾病,我们讨论了主要的临床和生化特征以及中风可能的发病机制,以及筛查和确诊所需的适当检测方法。导致中风的遗传疾病和机制种类繁多,这凸显了了解遗传疾病对于正确诊断和治疗影响儿童和成人的常见临床问题的重要性日益增加。

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