June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
Simultaneous expression of ABCA4 and USH2A mutations in one sporadic RP patient
Author Affiliations & Notes
  • Liping Yang
    Peking University Eye Center, Peking University Third Hospital, Beijing, China
  • Footnotes
    Commercial Relationships   Liping Yang, None
  • Footnotes
    Support  NSFC
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 2774. doi:
  • Views
  • Share
  • Tools
    • Alerts
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Liping Yang; Simultaneous expression of ABCA4 and USH2A mutations in one sporadic RP patient. Invest. Ophthalmol. Vis. Sci. 2017;58(8):2774.

      Download citation file:

      © ARVO (1962-2015); The Authors (2016-present)

  • Supplements

Purpose : To describe a complex, overlapping phenotype expressed in a sporadic RP patient who harboring pathogenic mutations in the ABCA4 and USH2A genes.

Methods : A specific hereditary eye disease enrichment panel (HEDEP) based on exome capture technology was used to collect the protein coding regions of 441 targeted hereditary eye disease genes, followed by high-throughput sequencing on the Illumina HiSeq2000 platform. Four potential disease causing mutations were identified. Segregation analysis was done in the available family members and a large cohort of controls with Sanger sequencing.

Results : Affected individuals presented with bull’s eye lesions and typical bone-spicule pigment deposition in the med-peripheral retina. HEDEP analysis demonstrated that the patient carried two compound heterozygous mutations both in ABCA4 (c.6088C>T;p.R2030* and c.5318C>T; p.A1773V ) and USH2A (c.4758+3A>G and c.1624A>G;p.S542G). The mutations p.R2030* and p.S542G were inherited from his father, and the mutations p.A1773V and c.4758+3A>G were inherited from his mother. Both his father and mother were unaffected.

Conclusions : An individual carrying both ABCA4 and USH2A disease-causing mutations can express a complex, overlapping phenotype associated with both Stargardt disease and RP.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.


This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.