1992
DOI: 10.1097/00000441-199205000-00010
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Case Report: Retinitis Pigmentosa Following Cytotoxic Chemotherapy in Usher’s Syndrome

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Cited by 8 publications
(3 citation statements)
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“…Retinitis pigmentosa, the most common hereditary retinal degeneration, typically begins with night blindness and may be associated with abnormal cilia and disrupted OS renewal (Young 1977;Arden and Fox 1979;Dryja and Berson 1995). The present study corroborates other recent research (Barrong et al 1992;Berson and Adamian 1992;Blanchet et al 1992;Weil et al 1995) supporting a ciliary pathology in some forms of retinitis pigmentosa: lower stability of the ciliary axoneme in rods than cones may contribute to the higher susceptibility of rods to degeneration.…”
Section: Resultssupporting
confidence: 92%
“…Retinitis pigmentosa, the most common hereditary retinal degeneration, typically begins with night blindness and may be associated with abnormal cilia and disrupted OS renewal (Young 1977;Arden and Fox 1979;Dryja and Berson 1995). The present study corroborates other recent research (Barrong et al 1992;Berson and Adamian 1992;Blanchet et al 1992;Weil et al 1995) supporting a ciliary pathology in some forms of retinitis pigmentosa: lower stability of the ciliary axoneme in rods than cones may contribute to the higher susceptibility of rods to degeneration.…”
Section: Resultssupporting
confidence: 92%
“…32 A case of apparent acceleration of retinitis pigmentosa with blindness following cytotoxic chemotherapy for non-Hodgkin's lymphoma has been reported. 33 The involved patient probably had Usher's syndrome (congenital sensorineural deafness).…”
Section: Posterior Segment Side Effectsmentioning
confidence: 99%
“…Second is the possibility that RP may also have been a consequence of chemotherapy, even though we consider this explanation highly unlikely. We are not aware of any chemotherapeutical agents proven to be associated with the development of RP, there is only one case study reporting acceleration of RP after chemotherapy in a patient with non-Hodgkin’s lymphoma [ 15 ]. As we have no previous ophthalmological documentation of the patient, it is not known whether RP existed prior to the chemotherapy.…”
Section: Discussionmentioning
confidence: 99%