We report a case of bilateral Retinitis Pigmentosa Simplex (RP) with a combination of unilateral Fuchs' Heterochromic Uveitis (FHU). Both of these entities are quite rare syndromes and coexistence of these entities in one patient is rarer than can be expected. Even though this rare coexistance came together in one patient, we found no hereditary factors to presume that both traits segregate independently.
CITATION STYLE
Yalvaç, I. S., Altintas, A. K., Gökdere, A., & Duman, S. (1998). Fuchs’ heterochromic uveitis associated with retinitis pigmentosa. Acta Ophthalmologica Scandinavica, 76(2), 243–244. https://doi.org/10.1034/j.1600-0420.1998.760225.x
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