Recurrent myocardial injury in a de novo SON mutation ZTTK syndrome patient: a case report

• Published in: BMC pediatrics Vol. 24; no. 1; pp. 232 - 8
• Main Authors: Cui, Lang, Zhen, Zhen, Chen, Xi, Li, Qirui, Gao, Lu, Yuan, Yue
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 02.04.2024; BioMed Central; BMC
• Subjects: Age; Arrhythmias, Cardiac; Cardiomyopathy; Case Report; Case reports; Cell cycle; Child; Clinical medicine; Complications and side effects; Congenital diseases; Consortia; Dehydrogenases; Diagnosis; Diseases; Electrocardiography; Enzymes; Eye Abnormalities; Failure to thrive; Families & family life; Female; Fever; Gene mutations; Genetic disorders; Genomes; Health aspects; Heart diseases; Heart rate; Heterozygote; Humans; Infections; Intellectual disabilities; Intellectual Disability - genetics; Intelligence tests; Kinases; Mutation; Myocardial injury; Myocarditis; Pediatric research; Pediatrics; Phenotype; Proteins; Relapse; Risk factors; SON gene; Ultrasonic imaging; ZTTK syndrome; China; SON gene; Case report; ZTTK syndrome; Myocardial injury
• ISSN: 1471-2431; 1471-2431
• DOI: 10.1186/s12887-024-04703-4

Zhu-Tokita-Takenouchi-Kim syndrome (ZTTK syndrome) is a severe multi-systemic developmental disorder, caused by variants in the SON gene. A patient diagnosed with ZTTK syndrome who carried a de novo SON mutation and exhibited recurrent myocardial injury was described in this case. A 7-year-old girl was admitted to the Cardiology Department of Beijing Children's Hospital in November 2019 due to myocardial injury following respiratory infection. She displayed elevated myocardial enzymes and severe T-wave changes on electrocardiogram. Over the past three years, she had experienced myocardial injury on three occasions. Additionally, she exhibited intellectual disability, congenital amblyopia, and dysmorphic facial features. Genetic analysis revealed a de novo heterozygous mutation c.3852_3856delGGTAT in the SON gene, which was confirmed by Sanger sequencing of her parents. She received anti-infection treatment and was administered metoprolol orally. Her condition was stable at the time of discharge. Over a 42-month follow-up period at the outpatient clinic, she complained intermittent fatigue and palpitation. The identified SON mutation, which plays a crucial role in heart development and mitochondrial function, may be associated with an increased susceptibility to myocardial injury or cardiomyopathy. This case report contributes novel insights into this rare condition and suggests the expansion of the ZTTK syndrome phenotype.