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Usher Syndrome, Retinosis Pigmentosa and Deafness, Case Report

Author

Listed:
  • Luis Javier Cárdenas-Lamas

    (Assigned Doctor to the Pediatric Ophthalmology and Strabismus Department of the High Specialty Ophthalmology Unit at the Hospital Civil de Guadalajara Fray Antonio Alcalde, Mexico)

  • Marisol à ñiguez-Soto

    (Assigned Doctor to the Oculofacial Plastic and Orbital Surgery Department of the High Specialty Ophthalmology Unit at the Hospital Civil de Guadalajara Fray Antonio Alcalde, Mexico)

  • Sandra Elizabeth Partida-Calderón

    (Ophthalmic Surgeon with High Specialty in Pediatric Ophthalmology and Strabismus, Mexico)

  • Luis Humberto Sepúlveda Tinajero

    (Ophthalmic Surgeon and second year Fellowship in Medical and Surgical Retina at the Hospital Civil de Guadalajara Fray Antonio Alcalde, Mexico)

  • Alejandro Sedano-Ramos

    (Assigned Doctor to the Pediatrics Department at the Hospital Civil de Guadalajara Fray Antonio Alcalde, Mexico)

Abstract

Usher syndrome is a group of clinically variable disorders, with recessive autosomal inheritance...

Suggested Citation

  • Luis Javier Cárdenas-Lamas & Marisol à ñiguez-Soto & Sandra Elizabeth Partida-Calderón & Luis Humberto Sepúlveda Tinajero & Alejandro Sedano-Ramos, 2021. "Usher Syndrome, Retinosis Pigmentosa and Deafness, Case Report," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 37(2), pages 29488-29492, July.
    • Handle: RePEc:abf:journl:v:37:y:2021:i:2:p:29488-29492
    DOI: 10.26717/BJSTR.2021.37.006013
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