| Literature DB >> 32816121 |
Ilenia Maini1,2, Edoardo Errichiello3, Stefano Giuseppe Caraffi1, Orsetta Zuffardi3, Livia Garavelli4, Simonetta Rosato1, Veronica Bizzarri1, Marzia Pollazzon1, Gabriele Trimarchi1, Gianluca Contrò1, Benedetta Cavirani1,5, Chiara Gelmini1, Manuela Napoli6, Claudio Moratti6, Rosario Pascarella6, Susanna Rizzi5, Carlo Fusco5.
Abstract
Basel-Vanagaite-Smirin-Yosef syndrome (BVSYS) is an extremely rare autosomal recessive genetic disorder caused by variants in the MED25 gene. It is characterized by severe developmental delay and variable craniofacial, neurological, ocular, and cardiac anomalies. Since 2015, through whole exome sequencing, 20 patients have been described with common clinical features and biallelic variants in MED25, leading to a better definition of the phenotype associated with BVSYS. We report two young sisters, born to consanguineous parents, presenting with intellectual disability, neurological findings, and dysmorphic features typical of BVSYS, and also with bilateral perisylvian polymicrogyria. The younger sister died at the age of 1 year without autoptic examination. Whole exome sequencing detected a homozygous frameshift variant in the MED25 gene: NM_030973.3:c.1778_1779delAG, p.(Gln593Argfs). This report further delineates the most common clinical features of BVSYS and points to polymicrogyria as a distinctive neuroradiological feature of this syndrome.Entities:
Keywords: Basel-Vanagaite-Smirin-Yosef syndrome; Intellectual disability; MED25; Multiple congenital anomalies; Neuropathy; Polymicrogyria; Thin corpus callosum
Year: 2020 PMID: 32816121 DOI: 10.1007/s10048-020-00625-2
Source DB: PubMed Journal: Neurogenetics ISSN: 1364-6745 Impact factor: 2.660