Leber’s congenital amaurosis. Case report
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Resumen
Leber’s congenital amaurosis is an heterogeneous and genetic clinical disorder characterized by severe loss of vision at birth. It accounts for 10 to 18% of congenital blindness cases. Some patients exhibit solely retinal blindness and show evidence of multi-systemic involvement. The presentation of this case includes bibliographic review of the subject, presentation of a clinical case and description of the importance of stomatologic handling of these patients. Knowledge and understanding of the disease as well as treatment sequels are paramount.
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Quintino Cintora, E., López Morales, P. M., & Mendoza Rosas, V. (2019). Leber’s congenital amaurosis. Case report. Revista Odontológica Mexicana Órgano Oficial De La Facultad De Odontología UNAM, 18(1). https://doi.org/10.22201/fo.1870199xp.2014.18.1 ING.69530
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