| Literature DB >> 35418825 |
Daniel Martín Fernández-Mayoralas1, Jacobo Albert2, Sara López-Martín2,3, Mar Jiménez de la Peña4, Ana Laura Fernández-Perrone1, Ana Jiménez de Domingo1, Beatriz Calleja-Pérez5, Mónica Martínez-García6, Sara Álvarez6, Alberto Fernández-Jaén1,7.
Abstract
Bi-allelic mutations in the TUBGCP4 gene have been recently associated with autosomal recessive microcephaly with chorioretinopathy. However, little is known about the genotype-phenotype characteristics of this disorder. Here, we describe a 5-year-old male patient with autism and a normal occipitofrontal circumference. No retinal abnormalities were observed. Brain MRI revealed the presence of enlarged sheaths of both tortuous optic nerves; both eyes had shorter axial lengths. Whole-exome sequencing in trio revealed synonymous TUBGCP4 variants in homozygous state: c.1746G>T; p.Leu582=. This synonymous variant has been previously described and probably leads to skipping of exon 16 of TUBGCP4. These results broaden the clinical spectrum of this new syndrome and suggest that TUBGCP4 bi-allelic mutations may underlie complex neurodevelopmental disorders.Entities:
Keywords: Autism; Intellectual disability; Recessive syndrome; TUBGCP4
Year: 2021 PMID: 35418825 PMCID: PMC8928183 DOI: 10.1159/000519365
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769