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乙胺嘧啶对印度人群中由2种未报道的己糖胺酶A基因突变引起的青少年型泰-萨克斯病的短期疗效。

Temporary Efficacy of Pyrimethamine in Juvenile-Onset Tay-Sachs Disease Caused by 2 Unreported HEXA Mutations in the Indian Population.

作者信息

Udwadia-Hegde Anaita, Hajirnis Omkar

机构信息

Pediatric Neurology, Jaslok Hospital and Research Centre, Mumbai, Maharashtra, India.

Pediatric Neurology, Bhaktivedanta Hospital and Research Centre, Thane, Maharashtra, India.

出版信息

Child Neurol Open. 2017 Jan 17;4:2329048X16687887. doi: 10.1177/2329048X16687887. eCollection 2017 Jan-Dec.

Abstract

BACKGROUND

Juvenile Tay-Sachs disease is rarer than other forms of Tay-Sachs disease and is usually seen in children between the age of 2 and 10 years. Pyrimethamine as a pharmacological chaperone was used to increase β-hexosaminidase A activity in this patient.

PATIENT

We describe a patient with Tay-Sachs disease from the Indian population, a juvenile case who presented with developmental regression starting at the age of three, initially with motor followed by language regression. She is currently incapacitated with severe behavioral issues.

CONCLUSION

This brief communication gives an insight into the efficacy of pharmacological chaperones. It also describes two unreported mutations in hexosaminidase A gene from the Indian population. After commencing Pyrimethamine, though initial benefits with increase in levels corresponded with briefly halting the motor regression, the observed increase was only transient and not associated with discernible beneficial neurological or psychiatric effects.

摘要

背景

青少年型泰-萨克斯病比其他形式的泰-萨克斯病更为罕见,通常见于2至10岁的儿童。在该患者中,使用乙胺嘧啶作为药理伴侣来提高β-己糖胺酶A的活性。

患者

我们描述了一名来自印度人群的泰-萨克斯病患者,这是一名青少年病例,从三岁开始出现发育倒退,最初是运动功能倒退,随后是语言功能倒退。她目前因严重的行为问题而丧失能力。

结论

这篇简短的通讯深入探讨了药理伴侣的疗效。它还描述了来自印度人群的己糖胺酶A基因中的两个未报道的突变。开始使用乙胺嘧啶后,虽然最初水平升高带来的益处与短暂停止运动功能倒退相对应,但观察到的升高只是短暂的,且与明显的有益神经或精神效应无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d38/5417282/566d51b162f3/10.1177_2329048X16687887-fig1.jpg

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