Groupe Hospitalier Pitie Salpetriere, Paris, France.
CNS Spectr. 2010 Apr;15(4):231-6. doi: 10.1017/s1092852900000067.
Cerebrotendinous xanthomatosis (CTX) is a rare inborn disorder of sterol storage with autosomal recessive inheritance and a variable clinical presentation. We describe two siblings with an early psychiatric presentation of CTX-associated attention-deficit/hyperactivity disorder and oppositional defiant disorder, also associated with a mild intellectual disability and major behavioral impairments. In both cases, treatment with chenodeoxycholic acid improved externalized symptoms and a partial recovery of cognitive impairments was observed. This suggests that CTX is potentially reversible, demonstrating the need for early diagnosis and treatment of this disorder before irreversible neurological lesions can occur.
脑腱性黄瘤病(CTX)是一种罕见的遗传性固醇贮积障碍疾病,呈常染色体隐性遗传,临床表现多样。我们描述了两例 CTX 相关注意缺陷多动障碍和对立违抗性障碍的早期精神科表现的同胞患者,他们还伴有轻度智力残疾和严重的行为障碍。在这两种情况下,使用鹅脱氧胆酸治疗均可改善外化症状,观察到认知障碍有部分恢复。这表明 CTX 具有潜在的可逆转性,这表明在发生不可逆转的神经损伤之前,需要对此类疾病进行早期诊断和治疗。