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Journal articles on the topic 'Peters’ anomaly'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

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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2

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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3

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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4

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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5

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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6

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

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7

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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8

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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9

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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10

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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11

Trifanenkova, I. G., A. V. Tereshchenko, A. A. Vydrina, and T. A. Ageeva. "Modern methods of diagnosing Peters anomaly." Russian ophthalmology of children, no. 1 (March 24, 2023): 33–38. http://dx.doi.org/10.25276/2307-6658-2023-1-33-38.

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Peters anomaly is a rare disease, significant in its consequences and leading to disability. According to the literature, Peters anomaly was recorded in approximately 700 cases in Russia, and around the world about 35,000 people have various forms of this pathology. The main cause of occurrence is the presence of a genetic mutation. The disease has a variety of phenotypic manifestations, differently interpreted by the authors depending on the research methods used and clinical experience. An important step in determining the optimal tactics and timing of surgical intervention for Peters anomal

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12

Doward, W., R. Perveen, I. C. Lloyd, A. E. A. Ridgway, L. Wilson, and G. C. M. Black. "A mutation in the RIEG1 gene associated with Peters’ anomaly." Journal of Medical Genetics 36, no. 2 (1999): 152–55. http://dx.doi.org/10.1136/jmg.36.2.152.

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Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome. We report a 3′ splice site mutation within the 3rd intron of the RIEG1 gene which is associated with unilateral Peters’ anomaly. The mutation is a single base substition of A to T at the invariant -2 site of the 3′ splice site. Peters’ anomaly, which is characterised by ocular anterior segment dysgenesis and central corneal opacification, is distinct from Rieger anomaly. This is the first description of a RIEG1 mutation associated with Peters’ anomaly.

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13

Laura Agnestasia and Julie Dewi I Barliana. "Optical Iridectomy as An Alternative Clear Visual Axis for Peters Anomaly." Ophthalmologica Indonesiana 47, no. 1 (2021): 110–14. http://dx.doi.org/10.35749/journal.v47i1.100164.

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   Introduction and objective: Peters anomaly is a rare congenital disease presented with central leukoma, iridocorneal adhesion, and with or without a cataractous lens. The presence of central leukoma will block the visual axis and lead to a disruption in normal visual development. Therefore, optical iridectomy, which can overcome the high incidence of graft failure in penetrating keratoplasty (PK), has been proposed as the alternative treatment to clear the visual axis. This study aims to show the outcome of optical iridectomy in patients with Peters’ anomaly.  Method

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14

Tabuchi, Akio, Masashi Matsuura, and Mitsuyoshi Hirokawa. "Three siblings with Peters' anomaly." Ophthalmic Paediatrics and Genetics 5, no. 3 (1985): 205–12. http://dx.doi.org/10.3109/13816818509006136.

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15

Eggink, C. A., C. M. Mooy, and A. Pinckers. "Peters' anomaly: an unusual case." Ophthalmic Paediatrics and Genetics 12, no. 1 (1991): 19–22. http://dx.doi.org/10.3109/13816819109023080.

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16

Snehi, Sagarika, Gaurav Gupta, and Sushmita Kaushik. "Corneal Remodeling in Peters Anomaly." Ophthalmology 128, no. 2 (2021): 287. http://dx.doi.org/10.1016/j.ophtha.2020.09.034.

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17

Myles, W. Michael, Michael E. Flanders, David Chitayat, and Seymour Brownstein. "Peters' Anomaly: A Clinicopathologic Study." Journal of Pediatric Ophthalmology & Strabismus 29, no. 6 (1992): 374–81. http://dx.doi.org/10.3928/0191-3913-19921101-10.

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18

Lee, Chia-Fwu, Beatrice Y. J. T. Yue, Jeffrey Robin, Shoichi Sawaguchi, and Joel Sugar. "Immunohistochemical Studies of Peters' Anomaly." Ophthalmology 96, no. 7 (1989): 958–64. http://dx.doi.org/10.1016/s0161-6420(89)32788-6.

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19

Shabeeb, Nadine M., David A. Plager, and Anita N. Haggstrom. "Peters anomaly in PHACE syndrome." Journal of American Association for Pediatric Ophthalmology and Strabismus 21, no. 4 (2017): 331–33. http://dx.doi.org/10.1016/j.jaapos.2017.04.010.

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20

Yarar, Coskun, Ayten Yakut, Nilgun Yildirim, Bilal Yildiz, and Hikmet Basmak. "Neuhauser syndrome and Peters?? anomaly." Clinical Dysmorphology 15, no. 4 (2006): 249–51. http://dx.doi.org/10.1097/01.mcd.0000228421.59166.82.

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21

Sagara, Takeshi, Maki Kozawa, Kayoko Ota, Yoichiro Fujitsu, Katsuyoshi Suzuki, and Teruo Nishida. "Pupillary block in Peters’ anomaly." Japanese Journal of Ophthalmology 52, no. 6 (2008): 504–5. http://dx.doi.org/10.1007/s10384-008-0590-2.

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22

VAN Schooneveld, M. J., J. W. Delleman, F. A. Beemer, and L. M. Bleeker-Wagemakers. "Peters' Anomaly and Systemic Defects." Archives of Ophthalmology 104, no. 8 (1986): 1130. http://dx.doi.org/10.1001/archopht.1986.01050200036031.

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23

Pleskova, A. V., V. R. Getadaryan, and A. Yu Panova. "Comparative analysis of the results of surgical treatment for Peters anomaly and sclerocornea in young children." Russian Ophthalmological Journal 18, no. 2 (2025): 90–94. https://doi.org/10.21516/2072-0076-2025-18-2-90-94.

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Purpose: to study and compare the results of primary penetrating keratoplasty (PKP) in young children with Peters’ anomaly and sclerocornea. Material and methods. The survival rates of the graft after primary PKP were studied in 58 children (67 eyes) under 5 years of age with congenital corneal opacity in Peters’ anomaly (43 patients) and sclerocornea (15 patients). The biological result of the surgery was assessed by the Kaplan — Meier method, which was used to determine the “survival” of the graft. The functional result (taking into account the child’s age) was estimated approximately: by th

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24

Soh, Yu Qiang, and Jodhbir S. Mehta. "Selective Endothelial Removal for Peters Anomaly." Cornea 37, no. 3 (2018): 382–85. http://dx.doi.org/10.1097/ico.0000000000001472.

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25

Martinet, Virginie, Pascal Dureau, Olivier Bergès, and Georges Caputo. "Vitreoretinal Dysplasia Masquerading as Peters’ Anomaly." European Journal of Ophthalmology 20, no. 1 (2010): 228–30. http://dx.doi.org/10.1177/112067211002000134.

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26

Trabucchi, G., A. Piantanida, F. Bandello, M. Freschi, P. Nucci, and R. Brancato. "Congenital aphakia in Peters' anomaly syndrome." Acta Ophthalmologica Scandinavica 75, no. 5 (2009): 595–97. http://dx.doi.org/10.1111/j.1600-0420.1997.tb00157.x.

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27

Bhandari, Ramanath, Sara Ferri, Beatrice Whittaker, Margaret Liu, and Douglas R. Lazzaro. "Peters Anomaly: Review of the Literature." Cornea 30, no. 8 (2011): 939–44. http://dx.doi.org/10.1097/ico.0b013e31820156a9.

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28

Kinning, Esther, and Margaret Barrow. "Arthrogryposis in association with Peters?? anomaly." Clinical Dysmorphology 17, no. 3 (2008): 177–79. http://dx.doi.org/10.1097/mcd.0b013e3282f4a127.

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29

Jun, Albert S., and John D. Gottsch. "Misspelling of Peters anomaly: Author reply." American Journal of Ophthalmology 135, no. 2 (2003): 261. http://dx.doi.org/10.1016/s0002-9394(02)01950-5.

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30

Salik, Irim, Abhishek Gupta, Arjun Tara, Gerald Zaidman, and Samuel Barst. "Peters anomaly: A 5‐year experience." Pediatric Anesthesia 30, no. 5 (2020): 577–83. http://dx.doi.org/10.1111/pan.13843.

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31

Kivlin, J. D., R. M. Fineman, A. S. Crandall, and R. J. Olson. "Peters' Anomaly and Systemic Defects-Reply." Archives of Ophthalmology 104, no. 8 (1986): 1130. http://dx.doi.org/10.1001/archopht.1986.01050200036032.

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32

Traboulsi, Elias I. "Peters' Anomaly and Associated Congenital Malformations." Archives of Ophthalmology 110, no. 12 (1992): 1739. http://dx.doi.org/10.1001/archopht.1992.01080240079035.

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33

Almarzouki, Hashem S., Alaa A. Tayyib, Hassan A. Khayat, et al. "Peters Anomaly in Twins: A Case Report of a Rare Incident with Novel Comorbidities." Case Reports in Ophthalmology 7, no. 3 (2016): 464–70. http://dx.doi.org/10.1159/000450571.

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Introduction: Peters anomaly is a rare developmental malformation involving the anterior segment of the eye, which culminates in amblyopia or congenital blindness. Multiple ocular and/or systemic malformations have been observed with this anomaly, and novel comorbidities continue to be reported. Case Presentation: The probands were monozygotic twin boys (twin I and twin II) born to consanguineous parents at 36 weeks of gestation. Coarse facial features and deep-seated eyes were noted at birth. At 6 months, ophthalmic examination revealed that both twins were unable to blink in response to ligh

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34

Chen, Wen-Si, Dao-Man Xiang, and Lan-Xiang Hu. "Ultrasound Biomicroscopy Detects Peters’ Anomaly and Rieger’s Anomaly in Infants." Journal of Ophthalmology 2020 (March 23, 2020): 1–10. http://dx.doi.org/10.1155/2020/8346981.

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Aim. Congenital corneal opacities (CCOs) are the major causes of early visual deprivation in infants. Balloon ultrasound biomicroscopy (UBM) examination is an effective method to diagnose CCO. However, whether it is suitable for children examination is still unknown. Methods. 26 Peters’ anomaly (PA) or Rieger’s anomaly (RA) infants with congenital corneal opacities (CCO) (40 eyes) underwent UBM examinations to study their imaging features. Results. Based on the results, they were divided into UBM Dx-Type I: Descemet’s membrane (DM) and endothelium have heterogenous or discontinuous echo accomp

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35

Gollamudi, Subba R., Elias I. Traboulsi, Wallace Chamon, Walter J. Stark, and Irene H. Maumenee. "Visual outcome after surgery for Peters' anomaly." Ophthalmic Genetics 15, no. 1 (1994): 31–35. http://dx.doi.org/10.3109/13816819409056908.

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36

Aquavella, James V. "Incidence of Peters Anomaly and Congenital Opacity." Cornea 34, no. 2 (2015): e4. http://dx.doi.org/10.1097/ico.0000000000000316.

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37

Rao, Kavita V., Merle Fernandes, Nibaran Gangopadhyay, Geeta K. Vemuganti, Sannapaneni Krishnaiah, and Virender S. Sangwan. "Outcome of Penetrating Keratoplasty for Peters Anomaly." Cornea 27, no. 7 (2008): 749–53. http://dx.doi.org/10.1097/ico.0b013e31816fe9a7.

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38

Hashemi, Hassan, Reza Ghaffari, and Masomeh Mohebi. "Posterior Lamellar Keratoplasty (DSAEK) in Peters Anomaly." Cornea 31, no. 10 (2012): 1201–5. http://dx.doi.org/10.1097/ico.0b013e31825697a4.

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39

Senthilkumar, Vijayalakshmi A., and Ambika Subramaniam. "A Curious Case of Aborted Peters Anomaly." TNOA Journal of Ophthalmic Science and Research 62, no. 3 (2024): 371. http://dx.doi.org/10.4103/tjosr.tjosr_90_24.

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40

Faras, Hadeel, Fayka Al-Raqum, and Dina Ramadan. "Classic Galactosemia Presenting with Unilateral Peters’ Anomaly." Medical Principles and Practice 19, no. 4 (2010): 324–26. http://dx.doi.org/10.1159/000312722.

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41

Harissi-Dagher, Mona, and Kathryn Colby. "Anterior Segment Dysgenesis: Peters Anomaly and Sclerocornea." International Ophthalmology Clinics 48, no. 2 (2008): 35–42. http://dx.doi.org/10.1097/iio.0b013e318169526c.

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42

DeRespinis, Patrick A., and Rudolph S. Wagner. "Peters' Anomaly in a Father and Son." American Journal of Ophthalmology 104, no. 5 (1987): 545–46. http://dx.doi.org/10.1016/s0002-9394(14)74118-2.

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43

Dolezal, Kara A., Brenda L. Bohnsack, Cagri G. Besirli, and Sayoko E. Moroi. "Management of glaucoma associated with Peters anomaly." Journal of American Association for Pediatric Ophthalmology and Strabismus 22, no. 4 (2018): e81. http://dx.doi.org/10.1016/j.jaapos.2018.07.298.

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44

Jain, Samiskha Fouzdar, Zena Ibrahim, and Mehmet C. Mocan. "Anatomic and visual outcomes in peters anomaly." Journal of American Association for Pediatric Ophthalmology and Strabismus 23, no. 4 (2019): e28-e29. http://dx.doi.org/10.1016/j.jaapos.2019.08.099.

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45

Khurram, Darakhshanda D., K. Jayaprakash Patil, Eva Gajdosova, A. Liasis, and Samer Hamada. "Ocular and systemic findings in Peters anomaly." Journal of American Association for Pediatric Ophthalmology and Strabismus 17, no. 1 (2013): e18-e19. http://dx.doi.org/10.1016/j.jaapos.2012.12.077.

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46

Hope, William C., Jose A. Cordovez, Jenina E. Capasso, et al. "Peters anomaly in cri-du-chat syndrome." Journal of American Association for Pediatric Ophthalmology and Strabismus 19, no. 3 (2015): 277–79. http://dx.doi.org/10.1016/j.jaapos.2015.01.018.

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47

Suwannaraj, Sirinya, Oriel Spierer, Kara M. Cavuoto, Ta Chang, Peter Chang, and Craig McKeown. "Outcome of optical iridectomy in Peters anomaly." Journal of American Association for Pediatric Ophthalmology and Strabismus 19, no. 4 (2015): e64. http://dx.doi.org/10.1016/j.jaapos.2015.07.206.

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48

Najjar, Dany M., Stephen P. Christiansen, Erick D. Bothun, and C. Gail Summers. "Strabismus and Amblyopia in Bilateral Peters Anomaly." Journal of American Association for Pediatric Ophthalmology and Strabismus 10, no. 3 (2006): 193–97. http://dx.doi.org/10.1016/j.jaapos.2006.01.006.

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49

Spierer, Oriel, Kara M. Cavuoto, Sirinya Suwannaraj, Craig A. McKeown, and Ta Chen Chang. "Outcome of optical iridectomy in Peters anomaly." Graefe's Archive for Clinical and Experimental Ophthalmology 256, no. 9 (2018): 1679–83. http://dx.doi.org/10.1007/s00417-018-4000-2.

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50

Kivlin, Jane D., John C. Carey, and Mark A. Richey. "Brachymesomelia and Peters anomaly: A new syndrome." American Journal of Medical Genetics 45, no. 4 (1993): 416–19. http://dx.doi.org/10.1002/ajmg.1320450403.

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