Clinical Case of Goldenhar Syndrome in Psychiatric Practice

A. Kovaleva
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引用次数: 1

Abstract

A clinical case of a rare genetic oculo-auriculo-vertebral syndrome (Goldenhar syndrome) is presented in a young man of 18 years old, who was first sent for examination and treatment to the psychiatric ward. A retrospective analysis of anamnestic information indicates the emergence of psychopathological disorders in childhood in the form of a delay in psychoverbal development, emotional immaturity, and delays in the development of social behavior. Subsequently, persistent encephalasthenic and neurosis-like disorders were complicated by the addition of affective disorders of the depressive-dysphoric type and psychotic disorders. The lack of a timely integrated therapeutic approach with the addition of psychopharmacotherapy, psychotherapy and social therapy led to the formation of specific personality changes in organic etiology with significant disorders in the emotional sphere (lability of emotions, irritability, outbursts of anger, constant resentment and dissatisfaction with others), a decrease in the level of cognitive activity and a tendency to chronic course of neurosis-like and affective disorders. A statement of persistent pronounced violations of mental functions during follow-up observation caused severe restrictions in the main areas of life (communication, behavior control, education, work) and social maladaptation of the patient, which was the basis for referral to medical and social examination with the establishment of a disability group.
精神病学实践中的高氏综合征临床一例
一个罕见的遗传性眼-耳-椎综合征(Goldenhar综合征)的临床病例出现在一个18岁的年轻人身上,他首先被送到精神科病房进行检查和治疗。回顾性分析的失忆症信息表明,精神病理障碍的出现在儿童的形式,在心理发展的延迟,情绪不成熟,在社会行为的发展延迟。随后,持续性脑衰弱和神经症样障碍合并抑郁-烦躁型情感性障碍和精神病性障碍。缺乏及时的综合治疗方法,加上精神药物治疗、心理治疗和社会治疗,导致在情感领域(情绪不稳定、易怒、愤怒爆发、持续怨恨和对他人不满)形成特定的有机病因性人格改变,认知活动水平下降,并倾向于慢性神经症和情感障碍。在后续观察期间,关于精神功能持续受到明显侵犯的陈述,导致患者在主要生活领域(沟通、行为控制、教育、工作)受到严重限制,社会适应能力下降,这是在成立残疾小组后进行医疗和社会检查的基础。
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