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莱施-奈恩综合征

Lesch-Nyhan Disease.

作者信息

Nyhan William L

机构信息

Department of Pediatrics University of California San Diego La Jolla CA 92093-0830, USA.

出版信息

J Hist Neurosci. 2005 Mar;14(1):1-10. doi: 10.1080/096470490512490.

Abstract

The first description of Lesch-Nyhan disease was in 1964; the first two patients were seen in 1963. The disease has caught the imagination of a variety of clinicians and scientists. The clinical picture is striking, combining spasticity, involuntary movements, and cognitive retardation with self-injurious behavior and the manifestations of gout. Biochemically, the overproduction of uric acid--the end product of purine metabolism--was, when measured, the largest ever seen. The disease is now well understood on a molecular basis. Enzyme analysis and mutational analysis have made available a full range of genetic testing, including diagnosis, carrier detection, and prenatal diagnosis. Therapy with allopurinol has been effective for those manifestations the disease shares with gout. Treatment for the neurological and behavioral features of the disease remains elusive.

摘要

莱施-奈恩病的首次描述是在1964年;1963年首次发现了前两名患者。这种疾病引起了众多临床医生和科学家的关注。其临床表现令人瞩目,兼具痉挛、不自主运动、认知迟缓、自伤行为以及痛风的症状。从生化角度来看,嘌呤代谢的终产物尿酸的过度生成量,经测量是有史以来最高的。如今,这种疾病在分子层面已得到充分了解。酶分析和突变分析使得一系列基因检测成为可能,包括诊断、携带者检测和产前诊断。对于该疾病与痛风共有的那些症状,使用别嘌呤醇进行治疗已见成效。然而,针对该疾病神经和行为特征的治疗方法仍难以寻觅。

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