Genetic of preimplantation diagnosis of dysmorphic facial features and intellectual developmental disorder (CHDFIDD) without congenital heart defects

• Published in: Molecular genetics & genomic medicine 2022-02, Vol.10 (2), p.e1863-n/a
• Main Authors: Cui, Xiangrong, Wu, Xueqing, Wang, Hongwei, Zhang, Sanyuan, Wang, Wei, Jing, Xuan
• Format: Article
• Language: English
• Subjects: Adult; Brain research; CDK13 gene; Cell cycle; CHDFIDD; Child; Congenital diseases; Cyclin-dependent kinases; Data analysis; Defects; Developmental disabilities; Developmental Disabilities - diagnosis; Developmental Disabilities - genetics; Diagnosis; Disease; Embryos; Female; Gene expression; Gene regulation; Genetic counseling; Genetic disorders; Genetic screening; Heart; Heart Defects, Congenital - genetics; Heredity; Humans; In vitro fertilization; Informed consent; Intellectual disabilities; Intellectual Disability - diagnosis; Intellectual Disability - genetics; Kinases; Learning disabilities; Male; Medical screening; Mutation; novel variant; Original; Parents & parenting; Patients; PGT‐M; Phenotype; Pregnancy; Preimplantation Diagnosis; Proteins; RNA polymerase; Signal transduction; Transcription; whole‐exome sequencing
• ISSN: 2324-9269; 2324-9269
• DOI: 10.1002/mgg3.1863

Background Cyclin‐dependent kinase 13 plays a critical role in the regulation of gene transcription. Recent evidence suggests that heterozygous variants in CDK13 are associated with a syndromic form of mental deficiency and developmental delay, which is inherited in an autosomal dominant manner. Methods A mentally retarded mother (33‐year‐old) and son (10‐year‐old boy) in our hospital with CDK13 variant (c.2149 (exon 4) G>A. p.Gly717Arg) were detected by whole‐exome sequencing (WES). All published CDK13 variant syndrome cases as of November 11, 2021, were searched, and their clinical information was recorded and summarized. Results We studied two patients in a Chinese family with a heterozygous constitutional CDK13 variant (c.2149 (exon 4) G>A. p.Gly717Arg), exhibiting the classical characteristics of dysmorphic facial features and intellectual developmental disorder (CHDFIDD, OMIM # 617360), without congenital heart defects. This is the first reported case of an adult patient with a CDK13 variant that gave birth to the next generation with the same variant. Preimplantation genetic testing for monogenic disease (PGT‐M) was performed for the proband and her husband with full informed consent and successfully blocked the inheritance of the disease. Conclusion Our study is of great significance for molecular diagnosis and genetic counseling of patients with CDHFIDD and extends the variant spectrum of CDK13. This is the first reported case of an adult patient with a CDK13 variant that gave birth to the next generation with the same variant. Our study is of great significance for molecular diagnosis and genetic counseling of patients with CDHFIDD and extends the variant spectrum of CDK13.