PedAM
Pediatric Disease Annotations & Medicines
| Disease | retinitis |
| Phenotype | C0456909|vision loss |
| Sentences | 11 |
| PubMedID- 25015354 | We recently assessed efficacy of high-dose dha supplementation to slow vision loss in patients with x-linked retinitis pigmentosa (xlrp) in a randomized clinical trial. |
| PubMedID- 22908283 | Thus, necrotic mechanisms involving rip kinase are crucial in cone cell death in inherited retinal degeneration, suggesting the rip kinase pathway as a potential target to protect cone-mediated central and peripheral vision loss in patients with retinitis pigementosa. |
| PubMedID- 21054389 | These data suggest that correlation of serum bilirubin levels with rate of vision loss in patients with retinitis pigmentosa could provide a useful strategy to test the hypothesis that cones die from oxidative damage in patients with retinitis pigmentosa. |
| PubMedID- 20591747 | Background: vision loss in retinitis pigmentosa (rp) is a slowly progressive and inexorable threat to patients' independence. |
| PubMedID- 26469750 | Purpose: docosahexaenoic acid (dha) was supplemented in a single-site, placebo-controlled, randomized clinical trial designed to slow vision loss associated with x-linked retinitis pigmentosa (xlrp); the dhax trial. |
| PubMedID- 21940737 | Background: recessive mutant alleles of myo7a, ush1c, cdh23, and pcdh15 cause non-syndromic deafness or type 1 usher syndrome (ush1) characterised by deafness, vestibular areflexia, and vision loss due to retinitis pigmentosa. |
| PubMedID- 19741248 | Purpose: vision loss due to retinitis pigmentosa affects an estimated 15 million people worldwide. |
| PubMedID- 23991031 | Ush1b is one of the most severe forms of ush that leads to severe congenital hearing impairment and progressive vision loss due to retinitis pigmentosa that manifests pre-pubertally [1]. |
| PubMedID- 22449032 | The hearing loss is sensorineural, whereas the vision loss is associated with retinitis pigmentosa (rp), a degeneration of the retinal cells. |
| PubMedID- 25695052 | It is found that mutations in the mt-atp6 gene result in neuropathy, ataxia, and retinitis pigmentosa, which lead to muscle weakness, vision loss, and the other features. |
| PubMedID- 26059674 | A continuous decline in consanguineous marriages among the jewish and arab populations in israel may have contributed to the decrease in the rate of vision loss due to retinitis pigmentosa in children. |
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