Relevant bibliographies by topics / Peters’ anomaly

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Peters’ anomaly'

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

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Journal articles on the topic "Peters’ anomaly"

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Sault, Robert W., and Jeffrey Sheridan. "Peters’ Anomaly." Ophthalmology and Eye Diseases 5 (January 2013): OED.S11142. http://dx.doi.org/10.4137/oed.s11142.

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While conducting medical aid in Mozambique, a 41 year old African male presented to our eye clinic complaining of visual impairment. The male was found to have Peters’ anomaly type 2, a rare congenital ocular malformation leading to sensory amblyopia and glaucoma.
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Nauman, G. O. H., A. Jünemann, and U. Schönherr. "Peters anomaly." Ophthalmology 105, no. 8 (1998): 1353. http://dx.doi.org/10.1016/s0161-6420(98)98008-3.

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Surapaneni, Krishna R., Michael C. Struck, and Paul O. Phelps. "Peters Anomaly." Ophthalmology 122, no. 6 (2015): 1130. http://dx.doi.org/10.1016/j.ophtha.2014.12.027.

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Jordan, T. "Peters' anomaly." British Journal of Ophthalmology 80, no. 6 (1996): 579–80. http://dx.doi.org/10.1136/bjo.80.6.579-a.

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Zhang, Ze, Nasreen A. Syed, and Wallace L. M. Alward. "Peters Anomaly." Ophthalmology Glaucoma 2, no. 4 (2019): 266. http://dx.doi.org/10.1016/j.ogla.2019.03.005.

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Zaidman, Gerald. "Peters' anomaly." Ophthalmic Genetics 25, no. 2 (2004): 157–58. http://dx.doi.org/10.1080/13816810490514423.

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Orenburkina, O. I., A. E. Babushkin, and I. R. Karachurina. "Ophthalmological manifestations of Peters anomaly (literature review)." Russian Journal of Clinical Ophthalmology 24, no. 4 (2024): 206–10. https://doi.org/10.32364/2311-7729-2024-24-4-7.

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In addition to hereditary, more often bilateral ocular symptoms associated with clinical manifestations such as central corneal opacification (leucoma) with iridocorneal and/or corneolenticular adhesions, Peters syndrome (or Peters anomaly) also represents various systemic abnormalities. Nowadays, variety of conditions termed as Peters anomaly has been extended, and it may include both unilateral and bilateral eye disorders with or without systemic lesions. Iridocorneal and corneolenticular adhesions associated with underlying iris dysgenesis, interrupt intraocular fluid outflow and often lead
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Cruysberg, Johannes R. M. "Misspelling of Peters anomaly." American Journal of Ophthalmology 135, no. 2 (2003): 260. http://dx.doi.org/10.1016/s0002-9394(02)01951-7.

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Heath, D. Heather, and M. Bruce Shields. "Glaucoma and Peters' anomaly." Graefe's Archive for Clinical and Experimental Ophthalmology 229, no. 3 (1991): 277–80. http://dx.doi.org/10.1007/bf00167884.

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Yokota, Chika, Kazuyuki Hirooka, Naoki Okada, and Yoshiaki Kiuchi. "Risk and Prognostic Factors for Glaucoma Associated with Peters Anomaly." Journal of Clinical Medicine 12, no. 19 (2023): 6238. http://dx.doi.org/10.3390/jcm12196238.

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Glaucoma secondary to Peters anomaly is an important factor affecting visual prognosis, but there are few reports on the condition. This study aimed to investigate the characteristics of glaucoma associated with Peters anomaly and glaucoma surgery outcomes. This retrospective study included 31 eyes of 20 patients with Peters anomaly. Peters anomaly was classified into three stages: Stage 1, with a posterior corneal defect only; Stage 2, a corneal defect with iridocorneal adhesion; and Stage 3, a corneal defect with lens abnormalities. The associations between glaucoma and anterior segment dysg
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Dissertations / Theses on the topic "Peters’ anomaly"

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Borrie, Adrienne E. "A mutation screen of NR2E1 in patients with aniridia, Peters' anomaly and related eye disorders." Thesis, University of British Columbia, 2009. http://hdl.handle.net/2429/17677.

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Aniridia is a rare genetic panocular (whole eye) disorder which, for the majority of cases, is caused by mutations or chromosomal rearrangements involving paired box gene 6 (PAX6). Peters’ anomaly (PA), also a genetic eye disorder, has also been found to be associated with mutations in PAX6, and also in FOXC1, PITX2, and CYP1B1. However, in approximately 20% of patients who have aniridia and 75% of patients with PA, no mutation has been found in PAX6, or other genes involved these eye disorders, and for these patients, their genetic mutation is unknown. This precludes these patients from genet
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Araújo, Carlos Jorge Trindade. "Molecular characterization of a de novo t (11;18) translocation associated with Peter´s anomaly." Master's thesis, Faculdade de Ciências e Tecnologia, 2013. http://hdl.handle.net/10362/11893.

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Dissertação para obtenção do grau de Mestre em Genética Molecular e Biomedicina<br>Peter’s anomaly (PA) is a congenital defect of the anterior chamber of the eye. The aim of this study is molecular characterization of a de novo balanced chromosome translocation [t(11;18)(q23.3;q11.2)] identified in a proband with syndromic form of Peter´s anomaly (ectopia lentis and mild CNS abnormalities). Chromosome breakpoints were identified at nucleotide resolution. The 11q23.3 breakpoint is at position 120,097,868 (genome assembly GRCh37/hg19) within intron 3 of out of first protein homolog gene (OAF) wh
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Döring, Andrea [Verfasser], and Peter [Akademischer Betreuer] Diedrich. "Die Untersuchung der Kiefergelenkfunktion bei Zahn- und Kieferfehlstellungen unter besonderer Berücksichtigung der Klasse-II-Anomalie / Andrea Döring ; Betreuer: Peter Diedrich." Aachen : Universitätsbibliothek der RWTH Aachen, 2001. http://d-nb.info/1214006515/34.

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Baquet, Moritz [Verfasser], Sohrab [Akademischer Betreuer] Fratz, Peter [Akademischer Betreuer] Ewert, and Alfred [Akademischer Betreuer] Hager. "Einfluss der Reduktion des rechtsventrikulären Volumens auf die kardiopulmonale Belastbarkeit: Ein Vergleich der korrigierten Fallot’schen Anomalie und der Ebstein Anomalie / Moritz Baquet. Betreuer: Sohrab Fratz. Gutachter: Peter Ewert ; Sohrab Fratz ; Alfred Hager." München : Universitätsbibliothek der TU München, 2016. http://d-nb.info/1097548058/34.

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Lemoine, Asseline. "Organisation et ségrégation lors de la formation de nanoalliages d'AgCo étudiés par diffusion aux petits et aux grands angles et effet anomal." Thesis, Orléans, 2015. http://www.theses.fr/2015ORLE2067/document.

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Ce travail de thèse a pour objectif d'étudier les rôles de la taille, de la composition et de la cinétique de croissance sur la morphologie, la structure, et l'état de mélange de l'argent et du cobalt dans des nanoparticules bimétalliques supportées AgCo. Dans ce but, des mesures in-situ et en temps réel par diffusion des rayons X aux petits et aux grands angles en géométrie d'incidence rasante, et en condition anomale, ont été effectuées au cours de la croissance des nanoparticules AgCo dans des conditions de dépôt simultané ou successif des métaux. Des recuits ont ensuite été réalisés afin d
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Pekala, Martha Sophia [Verfasser], Manfred O. [Akademischer Betreuer] Vogt, and Peter [Akademischer Betreuer] Ewert. "Hämodynamische Konsequenzen bei der Ebstein-Anomalie der Trikuspidalklappe : Eine vergleichende Studie an 76 Patienten und Probanden / Martha Sophia Pekala. Gutachter: Peter Ewert ; Manfred O. Vogt. Betreuer: Manfred O. Vogt." München : Universitätsbibliothek der TU München, 2014. http://d-nb.info/1060482614/34.

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Arm, Jakub. "Detekce anomálií běhu RTOS aplikace." Doctoral thesis, Vysoké učení technické v Brně. Fakulta elektrotechniky a komunikačních technologií, 2020. http://www.nusl.cz/ntk/nusl-432522.

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Due to higher requirements of computational power and safety, or functional safety ofequipments intended for the use in the industrial domain, embedded systems containing areal-time operating system are still the active area of research. This thesis addresses thehardware-assisted control module that is based on the runtime model-based verificationof a target application. This subsystem is intended to increase the diagnostic coverage,particularly, the detection of the execution errors. After the specification of the architecture,the formal model is defined and implemented into hardware using FP
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Ferreira, Vítor Emanuel Mendes. "Anomalia de Peters : revisão da literatura e descrição de caso clínico." Master's thesis, 2020. http://hdl.handle.net/10451/47518.

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Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Lisboa, 2020<br>A anomalia de Peters é uma disgenésia do segmento anterior do globo ocular caracterizada por opacidade central da córnea e sinéquias iridocorneanas. Apesar de ser uma patologia rara, está associada a uma morbilidade significativa, devido às alterações permanentes da visão, secundárias a ambliopia e glaucoma. Os principais objetivos deste trabalho incluem a descrição de um caso clínico de anomalia de Peters, suportado por uma revisão da literatura. Em primeiro lugar, é realizada uma
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Book chapters on the topic "Peters’ anomaly"

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Boente, Charline S., and Faruk H. Örge. "Peters Anomaly." In Practical Management of Pediatric Ocular Disorders and Strabismus. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2745-6_13.

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Arora, Monika, Ananya Kaginalkar, and Radhika Tandon. "Peters Anomaly with Glaucoma." In Childhood Glaucoma. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-19-7466-3_12.

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Valk, Rüdiger. "Deciphering the Co-Car Anomaly of Circular Traffic Queues Using Petri Nets." In Application and Theory of Petri Nets and Concurrency. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-76983-3_22.

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Khatri, N. K., and P. K. Chaudhury. "Interpreting Carbonates Generated AVO Anomaly in Clastic Regime: A Case Study in Deepwaters of Indian Basin." In Petro-physics and Rock Physics of Carbonate Reservoirs. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1211-3_15.

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"7 Peters Anomaly." In Wills Eye Handbook of Ocular Genetics, edited by Alex V. Levin, Mario Zanolli, and Jenina E. Capasso. Georg Thieme Verlag, 2018. http://dx.doi.org/10.1055/b-0037-149030.

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Parikh, Mansi, and Wallace L. M. Alward. "Axenfeld-Rieger Syndrome and Peters' Anomaly." In Cornea. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-323-06387-6.00065-9.

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Traboulsi, Elias I. "Eye." In Human Malformations and Related Anomalies Second Edition. Oxford University PressNew York, NY, 2005. http://dx.doi.org/10.1093/oso/9780195165685.003.0009.

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Abstract Ocular malformations can occur in isolation or accompany other systemic abnormalities in the context of malformation syndromes. Several ocular malformations can coexist, resulting in complex but well-defined clinical ocular phenotypes such as persistent hyperplastic primary vitreous or aniridia. Other malformations such as Peters anomaly and the morning glory disc anomaly are extremely variable in clinical appearance and have been given a number of descriptive names over the years because of a failure to recognize the spectrum in their morphology.
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Aoyagi, Amanda Mayumi, Isabele Ferreira da Silva, Amanda de Almeida Martins, et al. "Peters Syndrome: A diagnostic approach, clinical evolution and review." In Harmony of Knowledge: Exploring Interdisciplinary Synergie. Seven Editora, 2024. http://dx.doi.org/10.56238/sevened2023.006-143.

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Introduction: Peters syndrome (or Peters anomaly, or anterior segment mesenchymal dysgenesis) is a rare and congenital genetic condition, described by Arthur G. H. Peters in 1906, which affects the anterior ocular mesenchymal segment, presenting varying degrees of corneal opacity, iridocorneal synechiae, presence of anterior chamber narrowing and Descemet's membrane defect. Case Presentation: A 6-year-old boy, born in Goiânia, state of Goiás, with a term birth and no history of previous health problems, was referred to our service by a general practitioner due to reduced visual acuity (VA) pro
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Khan, Arif O. "Cornea Plana." In Genetic Diseases of the Eye, 3rd ed. Oxford University PressNew York, 2025. https://doi.org/10.1093/med/9780197659403.003.0009.

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Abstract Autosomal recessive cornea plana is a distinct congenital phenotype that is specific for biallelic pathogenic variants in the gene KERA. Classic features include corneal flattening, variable deep corneal opacity, indistinct limbus, variable iris abnormalities, high hyperopia, and accommodative esotropia. Although the anterior segment phenotype is pathognomonic, the condition may be misdiagnosed as Peters anomaly or microphthalmia. Rare features include corneal ectasia and endothelial decompensation. There may be a less severe autosomal dominant form, but no associated gene has been id
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Traboulsi, Elias I. "P." In A Compendium of Inherited Disorders and the Eye. Oxford University PressNew York, NY, 2005. http://dx.doi.org/10.1093/oso/9780195170962.003.0015.

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Abstract A maternal age effect has been described. This does not apply to 20% of cases, which are due to unbalanced translocations. In these families, the risk of recurrence is much higher. Trisomy 13 The critical region seems to be located in the portion 13q14 to terminus. 1 in 10,000 to 1 in 25,000 newborns Microcephaly and cerebral malformations, which may be very severe, such as holoprosencephaly Low-set ears Cleft lip and palate, often bilateral (80%) Polydactyly and clenched fist Rocker-bottom feet Rib abnormalities Severe cardiac malformations (80%) Renal and genital anomalies Microphth
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Conference papers on the topic "Peters’ anomaly"

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Sharif, Harris. "PP-055 Peter’s anomaly – a rare cause of visual impairment in paediatrics." In 11th Europaediatrics Congress, Antalya, Türkiye, 17 – 21 April 2024. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/bmjpo-2024-epac.199.

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Imad, Muhammad, Ian Cleland, Patrick McAllister, and Christopher Nugent. "Improving the accuracy of Anomaly Detection in Multimodal Sensors using 1D-CNN." In PETRA '24: The PErvasive Technologies Related to Assistive Environments Conference. ACM, 2024. http://dx.doi.org/10.1145/3652037.3652052.

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Liu, Jianbo, Dragan Djurdjanovic, and Jun Ni. "Identification and Anomaly Detection for PLC Controlled Automatic Tool Changer Using Timed Petri Net." In ASME 2007 International Manufacturing Science and Engineering Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/msec2007-31222.

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In this paper, a new method is proposed for incremental identification of Programmable Logic Controller (PLC) controlled tool changing process using available binary event logs obtained from the PLC. The identified discrete event model identified takes the form of a modified Timed Petri Net (TPN). A real time anomaly detection system is then constructed by synchronizing the identified TPN model with the actual tool changing process through the event sequence. Any discrepancies between the model and actual system are recognized as anomalies. The test results show that the diagnostic system auto
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Zorriassatine, Farbod, Emily Burton, Jacqueline Boyd, Abdallah Naser, and Ahmad Lotfi. "Cross-Species Insights: Drawing Lessons Between Bird Lameness Detection and Human Gait Anomaly Detection." In PETRA '24: The PErvasive Technologies Related to Assistive Environments Conference. ACM, 2024. http://dx.doi.org/10.1145/3652037.3663928.

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Cohen, Joseph, Baoyang Jiang, and Jun Ni. "Fault Diagnosis of Timed Event Systems: An Exploration of Machine Learning Methods." In ASME 2020 15th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/msec2020-8360.

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Abstract Especially common in discrete manufacturing, timed event systems often require a high degree of synchronization for healthy operation. Discrete event system methods have been used as mathematical tools to detect known faults, but do not scale well for problems with extensive variability in the normal class. A hybridized discrete event and data-driven method is suggested to supplement fault diagnosis in the case where failure patterns are not known in advance. A unique fault diagnosis framework consisting of signal data from programmable logic controllers, a Timed Petri Net of the norm
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Yahaya, Salisu Wada, Ahmad Lotfi, and Mufti Mahmud. "A similarity measure approach for identifying causes of anomaly in activities of daily living." In PETRA '19: The 12th PErvasive Technologies Related to Assistive Environments Conference. ACM, 2019. http://dx.doi.org/10.1145/3316782.3322783.

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Howedi, Aadel, Ahmad Lotfi, and Amir Pourabdollah. "A multi-scale fuzzy entropy measure for anomaly detection in activities of daily living." In PETRA '20: The 13th PErvasive Technologies Related to Assistive Environments Conference. ACM, 2020. http://dx.doi.org/10.1145/3389189.3397987.

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Arndt, Tobias, Max Conzen, Ingo Elsen, et al. "Anomaly Detection in the Metal-Textile Industry for the Reduction of the Cognitive Load of Quality Control Workers." In PETRA '23: Proceedings of the 16th International Conference on PErvasive Technologies Related to Assistive Environments. ACM, 2023. http://dx.doi.org/10.1145/3594806.3596558.

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Kayode, Babatope O., Karl D. Stephen, and Abdullah Kaba. "Application of Data Science Algorithms to Establish a Novel Parameterization Approach for Static and Dynamic Models." In SPE Symposium: Leveraging Artificial Intelligence to Shape the Future of the Energy Industry. SPE, 2023. http://dx.doi.org/10.2118/214476-ms.

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Abstract Numerical simulation results are the basis of numerous oil and gas field developments. We based the numerical simulation models (or dynamic models) on 3D geological models. We constructed a geological model using core and log data obtained from wells as inputs to create a reservoir prototype. This paper describes the applications of artificial intelligence (AI) algorithms for parameterization of static and dynamic modeling processes. Accordingly, a hypothetical 3D geological model was created, and porosity and permeability were distributed using sequential Gaussian simulation. Then, P
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