Relevant bibliographies by topics / Retinitis Pigmen­to­sa

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Academic literature on the topic 'Retinitis Pigmen­to­sa'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Retinitis Pigmen­to­sa"

1

Rusli, Richardo. "Retinitis Pigmentosa." Cermin Dunia Kedokteran 47, no. 7 (2020): 351. http://dx.doi.org/10.55175/cdk.v47i7.597.

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<p>Retinitis pigmentosa merupakan sekelompok penyakit degenerasi retina herediter yang ditandai oleh disfungsi progresif fotoreseptor disertai hilangnya sel secara progresif dan akhirnya menyebabkan atrofi beberapa lapisan retina. Beberapa kasus retinitis pigmentosa merupakan penyakit genetik yang diturunkan secara Mendel. Pada funduskopi, dapat ditemukan perubahan pigmen retina seperti bone spicules. ERG menunjukkan dominasi penurunan amplitudo gelombang-b dalam kondisi skotopik. Farmakoterapi vitamin A, Docosahexaenoic acid (DHA), lutein/zeaxanthin bertujuan untuk mengurangi morbiditas
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2

Abdul Sami Memon, Zaheer Sultan, Asma, Madiha Waseem, Naseem, and Fizzah Farooq. "Macular abnormalities in patients with Retinitis Pigmentosa." JMMC 15, no. 2 (2025): 119–22. https://doi.org/10.62118/jmmc.v15i2.501.

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Objective: To assess the frequency of macular abnormalities identified through OCT in individuals with retinitis pigmen-tosa.Methodology: This quantitative cross-sectional research was conducted in the Department of Ophthalmology at Civil Hospital Karachi. A total of 50 eyes from patients aged 18 to 65 years, diagnosed with retinitis pigmentosa (RP), were examined. The diagnosis of retinal pigmentosa was based on symptoms such as poor night vision or visual field loss, along with an ophthalmological assessment revealing mid-peripheral pigmentary changes, arteriolar narrowing, and a waxy pallor
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3

LAURENCE, J. Z., and ROBERT C. MOON. "FOUR CASES OF “RETINITIS PIGMEN-TOSA'” OCCURRING IN THE SAME FAMILY, AND ACCOMPANIED BY GENERAL IMPERFECTIONS OF DEVELOPMENT." Obesity Research 3, no. 4 (1995): 400–403. http://dx.doi.org/10.1002/j.1550-8528.1995.tb00166.x.

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4

Barton, Chris, Sabiha Kausar, Deborah Kerr, Stefania Bitetti, and Rob Wynn. "SIFD as a novel cause of severe fetal hydrops and neonatal anaemia with iron loading and marked extramedullary haemopoiesis." Journal of Clinical Pathology 71, no. 3 (2017): 275–78. http://dx.doi.org/10.1136/jclinpath-2017-204698.

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SIFD describes a heritable, syndromic condition characterised principally by sideroblastic anaemia (SA) with immunodeficiency, fevers and developmental delay, arising in mutations within the TRNT1 gene. Other clinical manifestations of SIFD include cardiomyopathy, seizures, sensorineural hearing loss, renal dysfunction, metabolic abnormalities, hepatosplenomegaly and retinitis pigmentosa.Presentation of SIFD is variable but typically in early childhood with SA or with fever. In this report, we extend the described SIFD phenotype. We describe a kindred in which the index case presented with fet
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5

Huang, Hui, Jing Wang, Haoran Li, et al. "Acupuncture for retinitis pigmentosa: study protocol for a randomised, sham-controlled trial." BMJ Open 11, no. 11 (2021): e049245. http://dx.doi.org/10.1136/bmjopen-2021-049245.

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IntroductionPrimary retinitis pigmentosa (RP) is a common hereditary retinal disease in ophthalmology that has a considerable impact on quality of life, but there are few effective therapeutic strategies. This trial aims to determine the efficacy and safety of acupuncture versus sham acupuncture (SA) for RP.Methods and analysisThis is a study protocol for a randomised, participant-blind, sham-controlled trial. 64 eligible patients with RP will randomly be divided into acupuncture group and SA group. All groups will receive 48 sessions over 3 months. Participants will complete the trial by visi
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6

Heutinck, Pam A. T., L. Ingeborgh van den Born, Jan A. M. van Laar, et al. "Somatostatin analogues as a treatment option for cystoid maculopathy in retinitis pigmentosa." BMJ Open Ophthalmology 9, no. 1 (2024): e001722. http://dx.doi.org/10.1136/bmjophth-2024-001722.

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AimsThis study aimed to evaluate the effectiveness of somatostatin analogues (SA) for cystoid maculopathy (CM) in retinitis pigmentosa (RP) patients.Materials and methodsIn this retrospective case series, clinical and imaging characteristics of 28 RP patients with CM, unresponsive to carbonic anhydrase inhibitors, were collected from medical charts. All patients received SA treatment as an alternative (octreotide long-acting release at 20 mg/month or 30 mg/month, or lanreotide at 90 mg/month or 120 mg/month). Outcome measures were mean reduction in foveal thickness (FT) and foveal volume (FV)
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7

Dwibedi, Tarun Kumar, Veerayya R. Hiremath, Shashikala K, and Gururaj N. "UNDERSTANDING THE CONCEPT OF PATALA & DRISHTI." International Ayurvedic Medical Journal 8, no. 10 (2020): 4841–46. http://dx.doi.org/10.46607/iamj4408102020.

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Language is the base of communication. Communication is made to understand and learn the mind and imagination. Ayurveda, the ancient life science is full of terminologies. To treat any disease, one should have thorough knowledge regarding those terminologies and their multiple meanings used in different con-texts. A very little description of Drishti and Patala are available in the classical literature regarding its measurement, shape, size and Panchabhoutiktwa, which is not sufficient to confine Drishti and Patala to any one part of eye. By analyzing different quotations of classical literatu
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8

Jung, Suk Hoon, Sang Un Yi, Bo-Een Hwang, Young Gun Park, and Young-Hoon Park. "Optical coherence tomography analysis at initial diagnosis in patients with retinitis pigmentosa and associated cystoid macular edema." PLOS One 20, no. 6 (2025): e0325654. https://doi.org/10.1371/journal.pone.0325654.

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This retrospective study analyzed optical coherence tomography (OCT) findings in 130 eyes of 130 patients with retinitis pigmentosa (RP) at initial diagnosis, including 42 with cystoid macular edema (CME) and 88 without, between September 2016 and March 2024. The CME group exhibited increased central macular thickness (CMT) (257.50 ± 104.98 µm vs. 171.40 ± 73.15 µm, p = 0.000), whereas the non-CME group had greater subfoveal choroidal thickness (SCT) (294.52 ± 122.85 µm vs. 246.98 ± 87.31 µm, p = 0.043), total choroidal area (TCA) (4.64 ± 1.98 mm² vs. 3.82 ± 1.34 mm², p = 0.031), stromal area
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9

de Bruijn, Suzanne E., Daan M. Panneman, Nicole Weisschuh, et al. "Identification of novel 3D-genome altering and complex structural variants underlying retinitis pigmentosa type 17 through a multistep and high-throughput approach." Frontiers in Genetics 15 (October 23, 2024). http://dx.doi.org/10.3389/fgene.2024.1469686.

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IntroductionAutosomal dominant retinitis pigmentosa type 17 (adRP, type RP17) is caused by complex structural variants (SVs) affecting a locus on chromosome 17 (chr17q22). The SVs disrupt the 3D regulatory landscape by altering the topologically associating domain (TAD) structure of the locus, creating novel TAD structures (neo-TADs) and ectopic enhancer-gene contacts. Currently, screening for RP17-associated SVs is not included in routine diagnostics given the complexity of the variants and a lack of cost-effective detection methods. The aim of this study was to accurately detect novel RP17-S
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