Zhang Liya, Liu Yu, Yan Lulu, Jin Xiamin, Zhu Lijiao, Yang Ting, Chen Lili, Cui Yingbo
Neonatal Center of Ningbo Women and Children's Hospital, Ningbo, Zhejiang 315012, China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 Jun 10;42(6):707-712. doi: 10.3760/cma.j.cn511374-20250108-00016.
To explore the clinical characteristics and genetic etiology of a child with Oral-facial-digital syndrome type Ⅰ(OFDSⅠ).
A child with OFDSⅠ who received treatment at the Women and Children's Hospital Affiliated to Ningbo University in March 2023 was selected as the study subject. A retrospective research method was used to collect the clinical data of the child. Peripheral venous blood samples were collected from the child, her parents and sister. Genomic DNA was extracted, and whole exome sequencing (WES) was performed. Candidate variants were validated using Sanger sequencing for familial verification. According to the Standards and Guidelines for the Interpretation of Sequence Variants developed by the American College of Medical Genetics and Genomics (ACMG) (hereinafter referred to as the "ACMG Guidelines"), the pathogenicity of the candidate variant was rated. This study was approved by the Medical Ethics Committee of Ningbo University Affiliated Women and Children's Hospital (Ethic No.: EC 2024-063).
The child was a prematurely born female with deformities of the oral cavity, fingers, and toes. She was admitted to the Neonatal Department of the Hospital where she was born due to shortness of breath 15 minutes after birth. The WES results indicated that the child has harbored a heterozygous c.710dup (p.Y238Vfs*2) frameshifting variant of the OFD1 gene. Sanger sequencing confirmed that neither of the child's parents nor her sister had carried the same variant. According to the ACMG guidelines, the variant was rated as pathogenic (PVS1+PS4_Moderate+PM2-Supporting+PM6_Supporting+PP4).
Children with OFDSⅠ have clinical features such as oral, finger, and toe deformities. The c.710dup (p.Y238Vfs*2) variant of the OFD1 gene probably underlay the OFDSⅠ in this child. Above result has enriched the mutational spectrum of the OFD1 gene.
探讨1例Ⅰ型口面指综合征(OFDSⅠ)患儿的临床特征及遗传病因。
选取2023年3月在宁波大学附属妇女儿童医院接受治疗的1例OFDSⅠ患儿作为研究对象。采用回顾性研究方法收集患儿的临床资料。采集患儿及其父母、姐姐的外周静脉血样本。提取基因组DNA,进行全外显子组测序(WES)。使用Sanger测序法验证候选变异,进行家系验证。根据美国医学遗传学与基因组学学会(ACMG)制定的《序列变异解释标准与指南》(以下简称“ACMG指南”)对候选变异的致病性进行评级。本研究经宁波大学附属妇女儿童医院医学伦理委员会批准(伦理编号:EC 2024 - 063)。
该患儿为早产女性,有口腔、手指和脚趾畸形。出生后15分钟因呼吸急促入住出生医院新生儿科。WES结果显示,该患儿携带OFD1基因的杂合c.710dup(p.Y238Vfs*2)移码变异。Sanger测序证实患儿的父母及姐姐均未携带相同变异。根据ACMG指南,该变异被评为致病性变异(PVS1+PS4_Moderate+PM2 - Supporting+PM6_Supporting+PP4)。
OFDSⅠ患儿具有口腔、手指和脚趾畸形等临床特征。OFD1基因的c.710dup(p.Y238Vfs*2)变异可能是该患儿患OFDSⅠ的原因。上述结果丰富了OFD1基因的突变谱。