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胍基乙酸甲基转移酶缺乏症患者的成功治疗:与治疗策略和病理生理学相关的发现

Successful treatment of a guanidinoacetate methyltransferase deficient patient: findings with relevance to treatment strategy and pathophysiology.

作者信息

Verbruggen Krijn T, Sijens Paul E, Schulze Andreas, Lunsing Roelineke J, Jakobs Cornelis, Salomons Gajja S, van Spronsen Francjan J

机构信息

Beatrix Children's Hospital, University Medical Centre Groningen, University of Groningen, The Netherlands.

出版信息

Mol Genet Metab. 2007 Jul;91(3):294-6. doi: 10.1016/j.ymgme.2007.03.006. Epub 2007 Apr 26.

Abstract

Biochemical and developmental results of treatment of a guanidinoacetate methyltransferase (GAMT) deficient patient with a mild clinical presentation and remarkable developmental improvement after treatment are presented. Treatment with creatine (Cr) supplementation resulted in partial normalization of cerebral (measured with magnetic resonance proton spectroscopy) and plasma levels of Cr and guanidinoacetate (GAA). Addition of high dose ornithine to the treatment led to further normalization of plasma GAA, while cerebral Cr and GAA did not improve further.

摘要

本文报道了对一名临床表现轻微且治疗后发育有显著改善的胍基乙酸甲基转移酶(GAMT)缺乏症患者的生化和发育治疗结果。补充肌酸(Cr)治疗使大脑(通过磁共振质子波谱测量)和血浆中的Cr及胍基乙酸(GAA)水平部分恢复正常。在治疗中添加高剂量鸟氨酸可使血浆GAA进一步恢复正常,而大脑中的Cr和GAA并未进一步改善。

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