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脑腱黄瘤病的精神表现。

Psychiatric manifestations in cerebrotendinous xanthomatosis.

机构信息

1] Federation of Neurology, La Salpêtrière Hospital, Groupe Hopsitalier Pitié-Salpêtrière (GHPS), Paris, France [2] Department of Neurogenetics, La Salpêtrière Hospital, Groupe Hopsitalier Pitié-Salpêtrière (GHPS), Paris, France.

出版信息

Transl Psychiatry. 2013 Sep 3;3(9):e302. doi: 10.1038/tp.2013.76.

Abstract

Cerebrotendinous xanthomatosis (CTX) is a rare and severe, but treatable, inborn disorder of bile acid biosynthesis and sterol storage with autosomal recessive inheritance and variable clinical presentation. CTX treatment consists of chenodeoxycholic acid and must be started as early as possible to prevent permanent disability. Psychiatric manifestations are rare and non-specific, and often lead to significant diagnostic and treatment delay. Therefore, better recognition of the gamut of psychiatric manifestations in CTX can diminish the risk of misdiagnosis and irreversible neurological deterioration. We hereby describe the psychiatric features in CTX. A complete review of all published cases of CTX in the medical literature was undertaken and the case reports with psychiatric presentation were collected and analyzed. We also describe the psychiatric features in relation to the neurological semeiology in six patients with CTX diagnosed at the La Salpêtrière Hospital. We conclude that psychiatric manifestations in CTX follow a bimodal/bitemporal pattern, appearing early in the disease course in the form of a behavioral/personality disorder associated with learning difficulties or mental retardation, or manifesting in advanced disease in the setting of dementia as rich neuropsychiatric syndromes, such as frontal, orbitofrontal or frontotemporal syndromes of cortico-subcortical dementia encompassing behavioral/personality disturbance, affective/mood disorders or psychotic disorders. Behavioral/personality disturbance in childhood or adolescence, especially when accompanied by learning difficulties, should therefore lead to further investigation to exclude CTX, as early diagnosis and treatment is critical for prognosis.

摘要

脑腱性黄瘤病(CTX)是一种罕见且严重但可治疗的遗传性胆汁酸生物合成和固醇储存障碍疾病,呈常染色体隐性遗传,临床表现多样。CTX 的治疗包括鹅脱氧胆酸,必须尽早开始,以防止永久性残疾。精神表现罕见且非特异性,常导致诊断和治疗延迟。因此,更好地认识 CTX 的各种精神表现可以降低误诊和不可逆神经恶化的风险。我们在此描述 CTX 的精神特征。对医学文献中所有已发表的 CTX 病例进行了全面回顾,并收集和分析了有精神表现的病例报告。我们还描述了在拉沙佩特里埃医院诊断为 CTX 的 6 名患者的神经症状学相关的精神特征。我们得出结论,CTX 的精神表现呈双峰/双时相模式,在疾病早期以行为/人格障碍的形式出现,伴有学习困难或智力迟钝,或在疾病晚期出现痴呆时表现为丰富的神经精神综合征,如额叶、眶额或额颞皮质下痴呆的皮质下痴呆综合征,包括行为/人格障碍、情感/情绪障碍或精神病障碍。因此,儿童或青少年时期出现的行为/人格障碍,尤其是伴有学习困难时,应进一步进行调查以排除 CTX,因为早期诊断和治疗对预后至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5433/3784765/ca1dac11e659/tp201376f1.jpg

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