Journal Article

The Expanding Phenotype of ZTTK Syndrome Due to the Heterozygous Variant of SON Gene Focusing on Liver Involvement: Patient Report and Literature Review

Lepri, Francesca Romana, Della Volpe, Luca, Della Corte, Claudia, Mosca, Antonella, Novelli, Antonio, Francalanci, Paola, Alterio, Tommaso, Maggiore, Giuseppe, Liccardo, Daniela, Figà Talamanca, Lorenzo, Monti, Lidia, Basso, Maria Sole, Pietrobattista, Andrea, Callea, Francesco, Veraldi, Silvio

2023

Overview

Zhu–Tokita–Takenouchi–Kim (ZTTK) syndrome, an intellectual disability syndrome first described in 2016, is caused by heterozygous loss-of-function variants in SON. Haploinsufficiency in SON may affect multiple genes, including those involved in the development and metabolism of multiple organs. Considering the broad spectrum of SON functions, it is to be expected that pathogenic variants in this gene can cause a wide spectrum of clinical symptoms. We present an additional ZTTK syndrome case due to a de novo heterozygous variant in the SON gene (c.5751_5754delAGTT). The clinical manifestations of our patient were similar to those present in previously reported cases; however, the diagnosis of ZTTK syndrome was delayed for a long time and was carried out during the diagnostic work-up of significant chronic liver disease (CLD). CLD has not yet been reported in any series; therefore, our report provides new information on this rare condition and suggests the expansion of the ZTTK syndrome phenotype, including possible liver involvement. Correspondingly, we recommend screening patients with SON variants specifically for liver involvement from the first years of life. Once the CLD has been diagnosed, an appropriate follow-up is mandatory, especially considering the role of SON as an emerging player in cancer development. Further studies are needed to investigate the role of SON haploinsufficiency as a downregulator of essential genes, thus potentially impairing the normal development and/or functions of multiple organs.

• Publisher: MDPI AG,MDPI
• Subject: carcinogenesis / Case Report / Cell cycle / Eye Diseases / Genes / Genetic disorders / Genomics / Genotype & phenotype / Haploinsufficiency / Hepatology / heterozygosity / Histology / Humans / Intellectual disabilities / Intellectual Disability - pathology / Laboratories / Literature reviews / liver / Liver - pathology / Liver cirrhosis / Liver diseases / loss-of-function mutation / Magnetic resonance imaging / metabolism / Mutation / patients / Pediatrics / Phenotype / Phenotypes / Stem cells / Syndrome / Ultrasonic imaging