| Literature DB >> 28272537 |
Francesco Testa1, Mariaelena Filippelli1, Raffaella Brunetti-Pierri1, Giuseppina Di Fruscio2, Valentina Di Iorio1, Mariateresa Pizzo3, Annalaura Torella2,3, Maria Rosaria Barillari4, Vincenzo Nigro2,3, Nicola Brunetti-Pierri3,5, Francesca Simonelli1, Sandro Banfi2,3.
Abstract
Mutations in the PCYT1A gene have been recently linked to two different phenotypes: one characterized by spondylometaphyseal dysplasia and cone-rod dystrophy (SMD-CRD) and the other by congenital lipodystrophy, severe fatty liver disease, and reduced HDL cholesterol without any retinal or skeletal involvement. Here, we identified, by next generation sequencing, sequence variants affecting function in the PCYT1A gene in three young patients with isolated retinal dystrophy from two different Italian families. A thorough clinical evaluation of the patients, with whole skeleton X-ray, metabolic assessment and liver ultrasound failed to reveal signs of skeletal dysplasia, metabolic and hepatic alterations. This is the first report showing that the PCYT1A gene can be responsible for isolated forms of retinal dystrophy, particularly without any skeletal involvement, thus further expanding the phenotypic spectrum induced by mutations in this gene.Entities:
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Year: 2017 PMID: 28272537 PMCID: PMC5392360 DOI: 10.1038/ejhg.2017.23
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246