SACS

SACS
  • 文章类型: Case Reports
    未经证实:Charcot-Marie-Tooth病(CMT)是最常见的遗传性神经肌肉疾病之一。SACS突变被证明会导致Charlevoix-Saguenay(ARSACS)的常染色体隐性遗传性痉挛性共济失调。然而,在越南患者中,关于CMT的NEFH和SACS基因突变的病例报道很少,CMT和ARSACS在临床上的诊断仍然重叠。
    未经证实:我们报告了两名表现为无小脑共济失调的感觉运动神经病的患者,痉挛和其他神经特征,通过电生理和临床检查和神经影像学诊断为中间型CMT。通过两个受影响成员的全外显子组测序小组,并对NEFH和SACS基因进行PCRSanger,以确认其父母上存在选定的变体,我们发现了一个新的错义变异NEFHc.1925C>T(遗传自母亲)在常染色体显性杂合状态,和两个隐性SACS变体(SACSc.13174C>T,导致错觉变异,和SACSc.11343del,在这两名患者中引起移码变异)(从母亲那里继承了一个,从父亲那里继承了另一个)。这些患者的临床和电生理发现与经典的ARSACS不匹配。据我们所知,这是2例受影响的兄弟姐妹被诊断为携带新型NEFH变异体和双等位基因SACS变异体的CMT的首例病例报告.
    UNASSIGNED:我们得出结论,这种新型NEFH变体可能是良性的,双等位基因SACS突变(c.13174C>T和c.11343del)可能是中间形式CMT的致病性。这项研究也有望强调中间形式CMT的当前知识,ARSACS,以及NEFH相关和SACS相关疾病的表型谱。我们希望对CMT有新的认识;然而,未来应进行进一步的研究,以提供对CMT发病机制的更透彻的认识。
    UNASSIGNED: Charcot-Marie-Tooth disease (CMT) is among the most common group of inherited neuromuscular diseases. SACS mutations were demonstrated to cause autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). However, there have been few case reports regarding to NEFH and SACS gene mutation to CMT in Vietnamese patients, and the diagnosis of CMT and ARSACS in the clinical setting still overlapped.
    UNASSIGNED: We report two patients presenting with sensorimotor neuropathy without cerebellar ataxia, spasticity and other neurological features, being diagnosed with intermediate form CMT by electrophysiological and clinical examination and neuroimaging. By whole-exome sequencing panel of two affected members, and PCR Sanger on NEFH and SACS genes to confirm the presence of selected variants on their parents, we identified a novel missense variant NEFH c.1925C>T (inherited from the mother) in an autosomal dominant heterozygous state, and two recessive SACS variants (SACS c.13174C>T, causing missense variant, and SACS c.11343del, causing frameshift variant) (inherited one from the mother and another from the father) in these two patients. Clinical and electrophysiological findings on these patients did not match classical ARSACS. To the best of our knowledge, this is the first case report of two affected siblings diagnosed with CMT carrying both a novel NEFH variant and biallelic SACS variants.
    UNASSIGNED: We concluded that this novel NEFH variant is likely benign, and biallelic SACS mutation (c.13174C>T and c.11343del) is likely pathogenic for intermediate form CMT. This study is also expected to emphasize the current knowledge of intermediate form CMT, ARSACS, and the phenotypic spectrum of NEFH-related and SACS-related disorders. We expect to give a new understanding of CMT; however, further research should be conducted to provide a more thorough knowledge of the pathogenesis of CMT in the future.
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  • 文章类型: Case Reports
    SACS基因的突变与CharlevoixSaguenay(ARSACS)的常染色体隐性遗传性痉挛性共济失调有关。它是一种临床和遗传异质性疾病,其特征是缓慢进行性共济失调,痉挛,感觉运动神经病,以及其他表现形式的组合,比如缺乏痉挛,听力损失,和癫痫发作。目前,关于中国患者SACS基因突变的病例报道很少。这里,我们描述了一名35岁的中国患者,在SACS中携带一种新的变异体(c.11486C>T),表现为进行性共济失调和脱髓鞘性周围神经病变.然后我们回顾了22例携带SACS基因突变的中国病例,包括我们的病人.他们都有小脑共济失调步态,并在脑磁共振成像(MRI)上显示小脑萎缩。在这些患者中鉴定出总共28个SACS突变。我们的研究进一步扩展了SACS基因的突变谱,并有助于评估基因型-表型相关性。
    Mutations in the SACS gene have been linked to autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS). It is a clinically and genetically heterogeneous disease characterized by slow progressive ataxia, spasticity, sensorimotor neuropathy, and a combination of other manifestations, such as lack of spasticity, hearing loss, and epileptic seizures. Currently, there have been very few case reports regarding the SACS gene mutation in Chinese patients. Here, we describe a 35-year-old Chinese patient carrying a novel variant in SACS (c.11486C>T) presenting with progressive ataxia and demyelinating peripheral neuropathy. We then reviewed 22 Chinese cases carrying SACS gene mutations, including our patient. All of them had a cerebellar ataxia gait and showed cerebellar atrophy on brain magnetic resonance imaging (MRI). A total of 28 SACS mutations were identified in these patients. Our study further expands the mutation spectrum of the SACS gene and contributes to the evaluation of genotype-phenotype correlations.
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  • 文章类型: Journal Article
    关于精神保健中的胁迫的研究最近已转向主观方面的研究,受影响的精神障碍患者和相关工作人员都站在一边。在这种情况下,越来越多地评估工作人员的个性特征和态度在胁迫决策中的作用。这项研究旨在研究在实验环境中,员工对胁迫的态度和员工的人格特质在围绕胁迫的决策中的作用。
    我们通过定量调查评估了精神病医院的精神卫生专业人员对胁迫和(一般)人格特质的态度。此外,我们制作了代表“灰色地带”案件的案例插图,并将其纳入调查,以评估工作人员在特定情况下关于胁迫的决定。
    在个别情况下,对胁迫的普遍认可态度极大地影响了围绕胁迫的决定-导致在小插曲中描述的情况下更有可能批准应用胁迫。人格特质似乎与此无关。
    减少精神病院胁迫的策略应更多地关注员工态度的作用,并鼓励员工批判性地反思。
    Research on coercion in mental healthcare has recently shifted to the investigation of subjective aspects, both on the side of the people with mental disorders affected and the staff members involved. In this context, the role of personality traits and attitudes of staff members in decision-making around coercion is increasingly being assessed. This study aimed to examine the role of staff attitudes towards coercion and staff members\' personality traits in decision-making around coercion in an experimental setting.
    We assessed the attitudes towards coercion and (general) personality traits of mental health professionals in psychiatric hospitals with a quantitative survey. Furthermore, we developed case vignettes representing cases in a \'grey zone\' and included them in the survey to assess staff members\' decisions about coercion in specific situations.
    A general approving attitude towards coercion significantly influenced decisions around coercion in individual cases-resulting in a more likely approval of applying coercion in the cases described in the vignettes. Personality traits did not seem to be relevant in this regard.
    Strategies to reduce coercion in mental healthcare institutions should focus more on the role of staff attitudes and encourage staff members to reflect on them critically.
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