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SOPH 综合征的起源:93 例雅库特患者的研究及 C 末端表型综述。

Origins of SOPH syndrome: A study of 93 Yakut patients with review of C-terminal phenotype.

机构信息

Research Laboratory of "Molecular Medicine and Human Genetics", Institute of Medicine, North-Eastern Federal University, Yakutsk, Russia.

Medical Genetic Center, Republic Hospital No1 - National Center of Medicine, Yakutsk, Russia.

出版信息

Clin Genet. 2023 Jun;103(6):625-635. doi: 10.1111/cge.14319. Epub 2023 Mar 21.

Abstract

Since the first report of SOPH syndrome among the Yakut population in 2010, new clinical data of SOPH-like conditions continue to appear. We expand the phenotypic spectrum of SOPH syndrome and perform a comparative analysis of Yakut SOPH patients' clinical data with SOPH-like conditions reported in the world scientific literature to form a foundation for NBAS pathogenesis discussion. Clinical data from the genetic records of 93 patients with SOPH syndrome and global survey data on patients with pathogenic variants of the C-terminal in the NBAS gene were collected. A detailed phenotype description of patients is presented with a total number of 111 individuals. Underweight below the fifth centile and prone to delayed bone age in Yakut SOPH patients are retrospectively observed. We outline the short stature with optic atrophy as the leading phenotyping trait for C-terminal NBAS patients. The pathophysiology and patients management of SOPH-like conditions are discussed.

摘要

自 2010 年在雅库特人群中首次报告 SOPH 综合征以来,新的 SOPH 样病症的临床数据不断出现。我们扩展了 SOPH 综合征的表型谱,并对雅库特 SOPH 患者的临床数据与世界科学文献中报道的 SOPH 样病症进行了比较分析,为 NBAS 发病机制的讨论奠定了基础。我们收集了 93 名 SOPH 综合征患者的遗传记录中的临床数据和 NBAS 基因 C 末端致病性变异患者的全球调查数据。我们总共对 111 个人进行了详细的表型描述。雅库特 SOPH 患者体重低于第五百分位数且易出现骨龄延迟的情况被回顾性观察到。我们总结了以视神经萎缩为主要表型特征的矮小身材的 C 末端 NBAS 患者。我们还讨论了 SOPH 样病症的病理生理学和患者管理。

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