Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, Leopoldina Hospital, 97422 Schweinfurt, Germany.
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Würzburg, 97080 Würzburg, Germany.
Int J Environ Res Public Health. 2020 Apr 29;17(9):3096. doi: 10.3390/ijerph17093096.
Partial deletion of chromosome 21q is a very rare genetic condition with highly variable phenotypic features including heart defects, high or cleft palate, brain malformations (e.g., cerebral atrophy), developmental delay and intellectual disability. So far, there is very limited knowledge about psychiatric disorders and their effective treatment in this special population. To fill this gap, the authors present the case of an initially five-year-old girl with distal deletion (del21q22.2) and comorbid oppositional defiant disorder (main psychiatric diagnosis) covering a period of time of almost four years comprising initial psychological/psychiatric assessment, subsequent treatment with Parent-Child Interaction Therapy (PCIT), and follow-up assessments. Post-intervention results including a 19-month follow-up indicated good overall efficacy of PCIT and high parental satisfaction with the treatment. This case report makes a substantial contribution to enhancing knowledge on psychiatric comorbidity and its effective treatment in patients with terminal 21q deletion. Moreover, it emphasizes the necessity of multidisciplinarity in diagnosis and treatment due to the variety of anomalies associated with 21q deletion. Regular screenings for psychiatric disorders and (if indicated) thorough psychological and psychiatric assessment seem to be reasonable in most affected children, as children with developmental delays are at increased risk of developing psychiatric disorders. As demonstrated with this case report, PCIT seems to be a good choice to effectively reduce disruptive behaviors in young children with partial deletion of chromosome 21q.
21q 染色体部分缺失是一种非常罕见的遗传病症,具有高度可变的表型特征,包括心脏缺陷、高腭或腭裂、脑畸形(如脑萎缩)、发育迟缓以及智力残疾。到目前为止,对于该特殊人群中的精神疾病及其有效治疗方法,我们的了解非常有限。为了填补这一空白,作者报告了一例最初五岁的女孩,患有远端缺失(del21q22.2)和共患对立违抗性障碍(主要精神诊断),时间跨度近四年,包括初始心理/精神评估、随后的亲子互动治疗(PCIT)以及随访评估。干预后的结果包括 19 个月的随访,表明 PCIT 的总体疗效良好,且父母对治疗非常满意。该病例报告对增强我们对患有 21q 末端缺失的患者的精神共病及其有效治疗的认识做出了重要贡献。此外,由于与 21q 缺失相关的各种异常,它强调了诊断和治疗的多学科性的必要性。对于大多数受影响的儿童,定期筛查精神疾病以及(如有必要)进行全面的心理和精神评估似乎是合理的,因为发育迟缓的儿童患精神疾病的风险增加。正如本病例报告所证明的那样,PCIT 似乎是治疗 21q 染色体部分缺失的幼儿破坏性行为的有效选择。