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以特征性认知和行为模式为线索,疑诊青春期前克氏综合征。

A characteristic cognitive and behavioral pattern as a clue to suspect Klinefelter syndrome in prepubertal age.

机构信息

Department of Pediatrics, University of Messina, Messina, Italy.

出版信息

J Am Board Fam Med. 2012 Sep-Oct;25(5):745-9. doi: 10.3122/jabfm.2012.05.110232.

Abstract

Klinefelter syndrome (KS) with the classic 47,XXY karyotype is the most frequent chromosomal aneuploidy, with a prevalence of 1 in 700 men; although the classic clinical picture is well-known and easily recognizable, most patients remain undiagnosed. The rate of diagnosis during childhood is extremely low, and only 10% of cases are identified before puberty, with a subsequent rate of ascertainment during lifetime of 25%. The low rate of timely diagnosis is because most of the classical signs and symptoms of androgen deficiency appear in mid- to late adolescence but it is important to recognize that adult men with KS may show a great variability in clinical and physical features. A common, often underappreciated, element in young boys and children with KS is the characteristic cognitive and behavioral pattern. We describe 2 patients who were diagnosed at 7.1 and 10 years through a characteristic neurocognitive profile. Both of them showed low-normal scores when evaluated by tests of general intelligence and a behavioral profile characterized by immaturity, low self-esteem, and learning disabilities. Clinical examination showed tall stature and progressive growth acceleration between 5 and 7 years, and one of them had hypoplastic scrotum with monolateral cryptorchidism. To achieve the goal of an early diagnosis of KS, it is necessary to increase medical awareness of the disease and, in particular, to augment pediatricians' knowledge that during prepubertal age pathognomonic clinical features of KS are often lacking but a characteristic cognitive and behavioral pattern is commonly present.

摘要

克氏综合征(KS),经典核型为 47,XXY,是最常见的染色体非整倍体,发病率为每 700 名男性中就有 1 例;尽管经典的临床特征广为人知且易于识别,但大多数患者仍未得到诊断。儿童时期的诊断率极低,只有 10%的病例在青春期前被发现,随后在一生中的检出率为 25%。低诊断率的原因是,大多数雄激素缺乏的典型体征和症状出现在从中年到青春期后期,但重要的是要认识到,KS 的成年男性可能在临床和身体特征上表现出很大的可变性。KS 患儿的一个常见但往往被低估的特征是其认知和行为模式。我们描述了 2 名患者,他们在 7.1 岁和 10 岁时通过典型的神经认知特征被诊断。他们的一般智力测试和行为特征评分均为低正常水平,行为特征表现为不成熟、低自尊和学习障碍。临床检查显示身材高大,5 至 7 岁期间生长加速,其中 1 名患者存在单侧隐睾的发育不良阴囊。为了实现 KS 的早期诊断目标,有必要提高对该病的医学认识,特别是增强儿科医生的认识,即青春期前 KS 的典型临床特征往往缺乏,但常见的是存在特征性认知和行为模式。

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