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A new look at XXYY syndrome: medical and psychological features.

机译:XXYY综合征的新外观:医学和心理特征。

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XXYY syndrome occurs in approximately 1:18,000-1:40,000 males. Although the physical phenotype is similar to 47,XXY (tall stature, hypergonadotropic hypogonadism, and infertility), XXYY is associated with additional medical problems and more significant neurodevelopmental and psychological features. We report on the results of a cross-sectional, multi-center study of 95 males age 1-55 with XXYY syndrome (mean age 14.9 years), describing diagnosis, physical features, medical problems, medications, and psychological features stratified by age groups. The mean age of diagnosis was 7.7 years. Developmental delays and behavioral problems were the most common primary indication for genetic testing (68.4%). Physical and facial features varied with age, although hypertelorism, clinodactyly, pes planus, and dental problems were common across all age groups. Tall stature was present in adolescents and adults, with a mean adult stature of 192.4 cm (SD 7.5; n = 22). Common medical problems included allergies and asthma (>50%), congenital heart defects (19.4%), radioulnar synostosis (17.2%), inguinal hernia and/or cryptorchidism (16.1%), and seizures (15%). Medical features in adulthood included hypogonadism (100%), DVT (18.2%), intention tremor (71%) and type II diabetes (18.2%). Brain MRI (n = 35) showed white matter abnormalities in 45.7% of patients and enlarged ventricles in 22.8%. Neurodevelopmental and psychological difficulties were a significant component of the behavioral phenotype, with developmental delays and learning disabilities universal but variable in severity. Twenty-six percent had full-scale IQs in the range of intellectual disability (MR), and adaptive functioning was significantly impacted with 68% with adaptive composite scores <70. Rates of neurodevelopmental disorders, including ADHD (72.2%), autism spectrum disorders (28.3%), mood disorders (46.8%), and tic disorders (18.9%), were elevated with 55.9% on psychopharmacologic medication overall. Recommendations for evaluation and treatment are summarized.
机译:XXYY综合征发生在大约1:18,000-1:40,000男性中。尽管物理表型与47,XXY(身材高,促性腺功能低下的性腺功能减退症和不育症)相似,但XXYY与其他医疗问题以及更重要的神经发育和心理特征有关。我们报告了一项针对95位XXYY综合征(平均年龄14.9岁)的1-55岁男性(年龄为14.9岁)的多中心横断面研究结果,其中描述了按年龄段分层的诊断,身体特征,医疗问题,药物和心理特征。平均诊断年龄为7.7岁。发育迟缓和行为问题是基因测试最常见的主要指征(68.4%)。身体和面部特征随年龄的变化而变化,尽管在所有年龄段中都存在超视,直视,扁平和牙齿问题。青少年和成年人的身高较高,平均成年人身高为192.4 cm(SD 7.5; n = 22)。常见的医学问题包括过敏和哮喘(> 50%),先天性心脏缺陷(19.4%),radio尺骨滑膜增生(17.2%),腹股沟疝和/或隐睾症(16.1%)和癫痫发作(15%)。成年期的医学特征包括性腺机能减退(100%),DVT(18.2%),意向性震颤(71%)和II型糖尿病(18.2%)。脑MRI(n = 35)在45.7%的患者中显示出白质异常,在22.8%的患者中显示出脑室扩大。神经发育和心理障碍是行为表型的重要组成部分,发育迟缓和学习障碍普遍存在,但严重程度却有所不同。 26%的人具有智商(MR)范围内的全面智商,并且适应性功能受到显着影响,其中68%的适应性综合得分<70。神经发育障碍的发生率,包括多动症(72.2%),自闭症谱系障碍(28.3%),情绪障碍(46.8%)和抽动障碍(18.9%),总体上在心理药物治疗中占55.9%。总结了评估和治疗的建议。

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