Fragile X Syndrome: A Rare Case of a Female Carrier Exhibiting the Phenotypic Spectrum of Disease Features

Yan Leyfman
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Abstract

Fragile X Syndrome is an X-linked recessive mutation in the Fragile X Mental Retardation 1 (FMR1) gene that results in CGG trinucleotide repeats in the 5’ untranslated arm of the FMR1 gene resulting in methylation that silences and/or reduces gene expression. The condition that manifests along a spectrum of symptoms depending on the number of repeats, where a premutation (defined as 55 to 200 CGG repeats) presents with less severe symptoms compared to a full mutation (>200 repeats). The full mutation tends to be more male predominant (85%), while the premutation tends to affect females more who are carrier of this condition [1]. The premutation condition is divided into two subtypesFragile X-associated Primary Ovarian Insufficiency (FXPOI) and Fragile X-associated Tremor/ Ataxia Syndrome (FXTAS) [2]. Although both conditions manifest with psychiatric conditions, they possess unique features on presentation where FXPOI occurs in 20% of female carriers and presents with menopause before the age of 40, while FXTAS occurs in 16% of females and presents with neurological symptoms, including intention tremors, ataxic gait, autonomic dysfunction, neuropathy, and Parkinsonism [3]. Although the psychiatric disorders common to both conditions tend to be depression and/or anxiety, they can also include psychosis and memory and executive function deficits in more advanced cases [4]. Studies have shown that in FXTAS the psychiatric symptoms manifest before the neurological conditions [5]. Studies have also noted an association between the cognitive decline in carriers of this mutation and increased substance abuse that patients fail to acknowledge as abnormal [6,7]. Due to the dearth of Fragile X carrier cases in the literature, there are few observed cases that can document the extent of this condition. Herein, we present a case of female adult carrier who has uniquely displayed the spectrum of systemic manifestations since menarche.
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脆性X综合征:罕见的女性携带者表现出疾病特征的表型谱
脆性X综合征是脆性X智力发育迟滞1 (FMR1)基因的X连锁隐性突变,导致FMR1基因5 '未翻译臂的CGG三核苷酸重复,导致甲基化,沉默和/或减少基因表达。根据重复次数表现出一系列症状的病症,其中预突变(定义为55至200个CGG重复)与完全突变(>200个重复)相比,症状较轻。全突变倾向于以男性为主(85%),而前置突变倾向于更多地影响携带该疾病的女性[1]。突变前状况分为脆性x相关性原发性卵巢功能不全(FXPOI)和脆性x相关性震颤/共济失调综合征(FXTAS)两种亚型[2]。虽然这两种疾病都表现为精神疾病,但它们在表现上有独特的特点,其中20%的女性携带者发生FXPOI,并在40岁前表现为绝经,而16%的女性患者发生FXTAS,并表现为神经系统症状,包括意图震颤、共济失调步态、自主神经功能障碍、神经病变和帕金森病[3]。虽然这两种情况的常见精神障碍往往是抑郁和/或焦虑,但在更晚期的病例中,它们也可能包括精神病、记忆和执行功能缺陷[4]。研究表明,在FXTAS患者中,精神症状先于神经系统疾病出现[5]。研究还指出,这种突变携带者的认知能力下降与患者未能认识到异常的药物滥用增加之间存在关联[6,7]。由于文献中缺乏脆性X基因携带者的病例,很少有观察到的病例可以记录这种情况的程度。在这里,我们提出了一个案例的女性成人载体谁独特地显示了系统表现频谱自初潮。
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