| Literature DB >> 30735726 |
Annarita Giliberti1, Aurora Currò1, Filomena Tiziana Papa2, Elisa Frullanti2, Francesca Ariani1, Gianni Coriolani3, Salvatore Grosso3, Alessandra Renieri4, Francesca Mari1.
Abstract
Myeloid ecotropic insertion site 2 (MEIS2) gene, encoding a homeodomain-containing transcription factor, has been recently related to syndromic intellectual disability with cleft palate and cardiac defects. Here, we present a male patient, aged 10, with cardiac defects, intellectual disability, facial dysmorphisms and gastroesophageal reflux. Whole exome sequencing revealed a novel de novo nonsense mutation in the MEIS2 gene. This patient represents another reported case with a de novo MEIS2 point mutation and helps to characterize a distinct facial phenotype consisting in low anterior hairline, thin eyebrows, anteverted nares, hypoplastic alae nasi, and M-shape upper lip. Furthermore, these data confirm the role of this gene in cardiac, nervous system development and gastrointestinal function.Entities:
Keywords: Exome analysis; Intellectual disability; MEIS2; Ventricular septal defect
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Year: 2019 PMID: 30735726 DOI: 10.1016/j.ejmg.2019.01.017
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708