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104例歌舞伎综合征患儿的临床特征及基因型-表型相关性:中国单中心横断面及随访研究

Clinical delineation and genotype-phenotype correlation in 104 children with kabuki syndrome: A single-center, cross-sectional and follow-up study in China.

作者信息

Wang Yirou, Hu Feihan, Xu Xueqiong, Tan Jun, Yu Tingting, Li Niu, Li Qian, Chen Yao, Chang Guoying, Ma Xiuqi, Yu Ding, Wang Xiumin

机构信息

Department of Endocrinology, Genetics and Metabolism, Shanghai Children'S Medical Center, School of Medicine, Shanghai Jiao Tong University, 1678 Dongfang Road, Shanghai, 200127, China.

Department of Endocrinology, Genetics and Metabolism, Shanghai Children'S Medical Center Guizhou Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 550081, GuiZhou, China.

出版信息

Eur J Pediatr. 2025 Mar 27;184(4):271. doi: 10.1007/s00431-025-06103-x.

Abstract

UNLABELLED

This study provides a detailed genotype and phenotype analysis of a large longitudinal cohort of Kabuki Syndrome (KS) from a single center in China. From July 2017 to July 2024, participants were enrolled at Shanghai Children's Medical Center. Variants in KMT2D or KDM6A were identified through whole exome sequencing. Phenotype data included prenatal and perinatal history, neonatal, childhood and adolescence evaluations. A total of 104 KS individuals fullfiled 362 outpatient visits, with an average follow-up of 2.58 years and a median follow-up time of 1.75 years. Growth curves were plotted based on 433 height data points. Among the patients, 27.08% had congenital heart defects (CHD), and 3 patients were identified with anomalous pulmonary venous connection as a new KS phenotype. KS patients showed facial feature heterogeneity, patients with atypical facial features associated with a older diagnosis age and a more diverse and severe phenotype. Among the 99 KS patients who provided facial photographs, the Face2Gene software was able to make accurate diagnoses in 85 individuals. The remaining 14 individuals may have had incorrect diagnoses because the provided photographs were not frontal facial images.

CONCLUSION

This study offered a comprehensive description of a Chinese KS cohort, and provided the first growth curves and a detailed CHD phenotype spectrum of Chinese KS patients. Our findings also suggest that, despite requirements for photograph quality, facial recognition software will be of significant value in the clinical diagnosis of KS.

WHAT IS KNOWN

• Kabuki syndrome is a rare disease that affects multiple systems. • Short stature is one of the common clinical manifestations of Kabuki syndrome.

WHAT IS NEW

• The genotypes and phenotypes of patients with Kabuki syndrome in China have been described in detail. • Growth curves for patients with Kabuki syndrome in China have been established.

摘要

未标注

本研究对来自中国单一中心的一大组卡布奇综合征(KS)纵向队列进行了详细的基因型和表型分析。2017年7月至2024年7月,参与者在上海儿童医学中心入组。通过全外显子组测序鉴定KMT2D或KDM6A中的变异。表型数据包括产前和围产期病史、新生儿、儿童期和青春期评估。共有104例KS患者完成了362次门诊就诊,平均随访2.58年,中位随访时间为1.75年。基于433个身高数据点绘制了生长曲线。患者中,27.08%患有先天性心脏病(CHD),3例患者被鉴定为肺静脉连接异常,这是一种新的KS表型。KS患者表现出面部特征异质性,具有非典型面部特征的患者诊断年龄较大,表型更多样化且更严重。在提供面部照片的99例KS患者中,Face2Gene软件能够对85例个体做出准确诊断。其余14例个体可能诊断有误,因为提供的照片不是正面面部图像。

结论

本研究全面描述了中国KS队列,并提供了中国KS患者的首条生长曲线和详细的CHD表型谱。我们的研究结果还表明,尽管对面部照片质量有要求,但面部识别软件在KS的临床诊断中将具有重要价值。

已知信息

• 卡布奇综合征是一种影响多个系统的罕见疾病。

• 身材矮小是卡布奇综合征的常见临床表现之一。

新发现

• 详细描述了中国卡布奇综合征患者的基因型和表型。

• 建立了中国卡布奇综合征患者的生长曲线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5c9/11950074/15316729ada5/431_2025_6103_Fig1_HTML.jpg

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