Briegel W
Department of Child and Adolescent Psychiatry and Psychotherapy, Bezirkskrankenhaus Passau, Passau, Germany.
Clin Genet. 2006 Aug;70(2):91-7. doi: 10.1111/j.1399-0004.2006.00649.x.
Möbius sequence is a rare condition of heterogeneous, and in most cases, unclear; origin, usually defined as a unilateral or bilateral congenital facial weakness with impairment of ocular abduction, which is frequently associated with limb anomalies. Disturbances in psychomotor and speech development are very common, and mental retardation is estimated to occur in 10-15% of cases. The incidence of autistic spectrum disorders might be increased in patients with Möbius sequence. After a brief overview on aetiology and physical appearance, current knowledge of cognitive capacities and academic achievement; psychomotor development; development of speech, language and communication; behaviour problems; psychiatric comorbidity and possible therapeutic interventions are reviewed.
莫比乌斯序列是一种罕见的、病因多样且大多不明的病症;其起源通常被定义为单侧或双侧先天性面部无力并伴有眼球外展障碍,常与肢体异常相关。精神运动和言语发育障碍非常常见,据估计10%-15%的病例会出现智力迟钝。莫比乌斯序列患者患自闭症谱系障碍的几率可能会增加。在对病因和外貌进行简要概述之后,本文将综述目前关于认知能力和学业成就、精神运动发育、言语、语言和交流发育、行为问题、精神共病以及可能的治疗干预措施的知识。