Articles | Volume 4, issue 2
https://doi.org/10.5194/pb-4-215-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/pb-4-215-2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
A review on ocular findings in mouse lemurs: potential links to age and genetic background
Marko Dubicanac
Institute of Zoology, University of Veterinary Medicine Hannover,
Buenteweg 17, 30559 Hannover, Germany
Ute Radespiel
Institute of Zoology, University of Veterinary Medicine Hannover,
Buenteweg 17, 30559 Hannover, Germany
Elke Zimmermann
CORRESPONDING AUTHOR
Institute of Zoology, University of Veterinary Medicine Hannover,
Buenteweg 17, 30559 Hannover, Germany
Related subject area
Pathology
Multiple adenomas of the thyroid gland in an African green monkey (Chlorocebus aethiops)
Spontaneous (Hashimoto-like) chronic lymphocytic thyroiditis in a rhesus macaque (Macaca mulatta)
Reactive mesothelial hyperplasia mimicking mesothelioma in an African green monkey (Chlorocebus aethiops)
Spontaneous meningioma in a pig-tailed macaque (Macaca nemestrina)
Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
Morphological and immunohistochemical characterization of spontaneous endometriosis in rhesus macaques (Macaca mulatta)
Unique case of granulomatous arteritis in a grey mouse lemur (Microcebus murinus) – first case description
A case of gallstones in an African green monkey (Chlorocebus aethiops)
Intravascular T-cell lymphoma in a patas monkey (Erythrocebus patas)
Spontaneous lung pathology in a captive common marmoset colony (Callithrix jacchus)
The Department of Pathology at the German Primate Center from 1973 to 1999
From the working group "Experimental Pathology" to the department "Pathology Unit" – historical development in retrospect
Unique case of disseminated toxoplasmosis and concurrent hepatic capillariasis in a ring-tailed lemur: first case description
Roland Plesker and Kernt Köhler
Primate Biol., 10, 1–6, https://doi.org/10.5194/pb-10-1-2023, https://doi.org/10.5194/pb-10-1-2023, 2023
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To our knowledge, this report represents the first description of thyroid gland tumors in an African Green Monkey (Chlorocebus aethiops). Two cystadenomas as well as a solid follicular adenoma are described in a 27-year-old female. No indications of excessive hormone production due to the tumors were detected.
Roland Plesker and Gudrun Hintereder
Primate Biol., 8, 37–42, https://doi.org/10.5194/pb-8-37-2021, https://doi.org/10.5194/pb-8-37-2021, 2021
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To our knowledge, this study is the first report of spontaneous Hashimoto-like chronic lymphocytic thyroiditis in a rhesus macaque (Macaca mulatta). Despite the microscopic similarities to human cases, autoantibodies (thyroglobulin antibodies, thyriod peroxidase antibodies, and thyroid-stimulating hormone receptor antibodies) were not identified in this rhesus macaque using a human electrochemiluminescence immunoassay system.
Roland Plesker, Kernt Köhler, Susanne von Gerlach, Klaus Boller, Markus Vogt, and Inke S. Feder
Primate Biol., 7, 5–12, https://doi.org/10.5194/pb-7-5-2020, https://doi.org/10.5194/pb-7-5-2020, 2020
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This report describes a reactive mesothelial hyperplasia as a reaction to a polyserositis in an African green monkey (Chlorocebus aethiops) mimicking an epitheloid mesothelioma. Histopathology, immunohistochemistry, fluorescence in situ hybridization, and electron microscopy were used to determine the benign nature of the mesothelial proliferation. For the first time, human genetic probes had been successfully applied to an African green monkey.
Roland Plesker, Martina Bleyer, and Kerstin Mätz-Rensing
Primate Biol., 5, 7–13, https://doi.org/10.5194/pb-5-7-2018, https://doi.org/10.5194/pb-5-7-2018, 2018
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We present a spontaneous tumor of the meninges (meningioma) in a female pig-tailed macaque (Macaca nemestrina) more than 24 years old. Clinically, the monkey displayed slow, weak, and insecure movements and poor vision. A tumorous mass was present at the floor of the cranial cavity. It compressed adjacent parts of the brain, infiltrated surrounding bones, and expanded into the throat. Microscopically, the tumor showed both meningothelial and microcystic parts.
Ivanela Kondova, Gerco Braskamp, Peter J. Heidt, Wim Collignon, Tom Haaksma, Nanine de Groot, Nel Otting, Gaby Doxiadis, Susan V. Westmoreland, Eric J. Vallender, and Ronald E. Bontrop
Primate Biol., 4, 117–125, https://doi.org/10.5194/pb-4-117-2017, https://doi.org/10.5194/pb-4-117-2017, 2017
Eva Gruber-Dujardin, Martina Bleyer, and Kerstin Mätz-Rensing
Primate Biol., 4, 77–91, https://doi.org/10.5194/pb-4-77-2017, https://doi.org/10.5194/pb-4-77-2017, 2017
Nicole Cichon, Karen Lampe, Felix Bremmer, Tamara Becker, and Kerstin Mätz-Rensing
Primate Biol., 4, 71–75, https://doi.org/10.5194/pb-4-71-2017, https://doi.org/10.5194/pb-4-71-2017, 2017
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We herein report a unique case of granulomatous arteritis in a grey mouse lemur affecting multiple organs, which is not comparable to other disease entities formerly described in nonhuman primates. The features of the entity most closely resemble disseminated visceral giant cell arteritis in humans. A concise description of the disease is given, and the differential diagnoses are discussed. An idiopathic pathogenesis is suspected.
Dina Kleinlützum and Roland Plesker
Primate Biol., 4, 33–37, https://doi.org/10.5194/pb-4-33-2017, https://doi.org/10.5194/pb-4-33-2017, 2017
Karen Lampe, Jens-Christian Rudnick, Fabian Leendertz, Martina Bleyer, and Kerstin Mätz-Rensing
Primate Biol., 4, 39–46, https://doi.org/10.5194/pb-4-39-2017, https://doi.org/10.5194/pb-4-39-2017, 2017
Martina Bleyer, Marius Kunze, Eva Gruber-Dujardin, and Kerstin Mätz-Rensing
Primate Biol., 4, 17–25, https://doi.org/10.5194/pb-4-17-2017, https://doi.org/10.5194/pb-4-17-2017, 2017
M. Brack
Primate Biol., 2, 81–87, https://doi.org/10.5194/pb-2-81-2015, https://doi.org/10.5194/pb-2-81-2015, 2015
F.-J. Kaup
Primate Biol., 2, 57–63, https://doi.org/10.5194/pb-2-57-2015, https://doi.org/10.5194/pb-2-57-2015, 2015
N. Siskos, K. Lampe, F.-J. Kaup, and K. Mätz-Rensing
Primate Biol., 2, 9–12, https://doi.org/10.5194/pb-2-9-2015, https://doi.org/10.5194/pb-2-9-2015, 2015
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In this paper, a co-infection with Toxoplasma gondii and Capillaria hepatica in a ring-tailed lemur is described. As a protozoan parasite, T. gondii can affect nearly all warm-blooded species, causing toxoplasmosis. In lemurs, toxoplasmosis has severe clinical manifestations leading to death. C. hepatica also affects a broad range of mammals, causing hepatic capillariasis. Although it is not known to be lethal, its potential predisposition to toxoplasmosis in our case is of great interest.
Cited articles
Abdelkader, H., Alany, R. G., and Pierscionek, B.: Age-related cataract and drug therapy: opportunities and challenges for topical antioxidant delivery to the lens, J. Pharm. Pharmacol., 67, 537–550, https://doi.org/10.1111/jphp.12355, 2015.
Akpek, E. K. and Gottsch, J. D.: Herpes zoster sine herpete presenting with hyphema, Ocul. Immunol. Inflamm., 8, 115–118, 2000.
Alves, M., Malki, L. T., and Rocha, E. M.: Buphthalmos development in adult: case report, Arq. Bras. Oftalmol., 75, 361–362, 2012.
Anninger, W. V., Lomeo, M. D., Dingle, J., Epstein, A. D., and Lubow, M.: West Nile virus-associated optic neuritis and chorioretinitis, Am. J. Ophthalmol., 136, 1183–1185, 2003.
Arentsen, J. J. and Green, W. R.: Melanoma of the iris: report of 72 cases treated surgically, Ophthalmic Surg., 6, 23–37, 1975.
Atipo-Tsiba, P. W. and Kombo Bayonne, E. S.: Immune reconstitution inflammatory syndrome and shingles associated with a combined paralysis of three oculomotor nerves: a case report, Ethiop. J. Health Sci., 26, 297–300, 2016.
Austad, S. N. and Fischer, K. E.: The development of small primate models for aging research, Ilar. J., 52, 78–88, 2011.
Beltran, W. A., Vanore, M., Ollivet, F., Nemoz-Bertholet, F., Aujard, F., Clerc, B., and Chahory, S.: Ocular findings in two colonies of gray mouse lemurs (Microcebus murinus), Vet. Ophthalmol., 10, 43–49, https://doi.org/10.1111/j.1463-5224.2007.00491.x, 2007.
Bonomi, L., Marchini, G., Marraffa, M., Bernardi, P., De Franco, I., Perfetti, S., Varotto, A., and Tenna, V.: Prevalence of glaucoma and intraocular pressure distribution in a defined population. The Egna-Neumarkt Study, Ophthalmology, 105, 209–215, 1998.
Bouzidi, A., Iferkhass, S., El Abidine Hansali, Z., Elmallaoui, M., and Laktaoui, A.: Exophthalmos of the left eye in favor of orbital adenoid cystic carcinoma: report of a case, Pan. Afr. Med. J., 22, 168, https://doi.org/10.11604/pamj.2015.22.168.7134, 2015.
Bowers, B., Gupta, D., Patel, H., and Mirza, N.: Exophthalmos as a presenting manifestation of limited Wegener's granulomatosis in a patient with prior graves' disease, Clin. Med. Case Rep., 2, 35–37, 2009.
Brenkman, R. F., Oosterhuis, J. A., and Manschot, W. A.: Recurrent hemorrhage in the anterior chamber caused by a (juvenile) xanthogranuloma of the iris in an adult, Doc. Ophthalmol., 42, 329–333, 1977.
Brockmann, T., Rossel, M., and Salchow, D. J.: Progressive idiopathic tractional corectopia with iris thinning, J. Aapos., 20, 464–466, https://doi.org/10.1016/j.jaapos.2016.06.010, 2016.
Burton, M., Habtamu, E., Ho, D., and Gower, E. W.: Interventions for trachoma trichiasis, Cochrane Db. Syst. Rev., 11, CD004008, https://doi.org/10.1002/14651858.CD004008.pub3, 2015.
Cayetanot, F., Van Someren, E. J., Perret, M., and Aujard, F.: Shortened seasonal photoperiodic cycles accelerate aging of the diurnal and circadian locomotor activity rhythms in a primate, J. Biol. Rhythm., 20, 461–469, https://doi.org/10.1177/0748730405279174, 2005.
Chi, M. J., Roh, J. H., Lee, J. H., and Paik, H. J.: A case of orbital lipoma with exophthalmos and visual disturbance, Jpn. J. Ophthalmol., 53, 442–444, https://doi.org/10.1007/s10384-009-0679-2, 2009.
Chousterman, B., Gualino, V., Dohan, A., and Payen, D.: A mysterious post-traumatic pulsatile exophthalmos, Intens. Care. Med., 40, 102–103, https://doi.org/10.1007/s00134-013-3076-8, 2014.
Coles, W. H.: Traumatic hyphema: an analysis of 235 cases, South. Med. J., 61, 813–816, 1968.
Colton, T. and Ederer, F.: The distribution of intraocular pressures in the general population, Surv. Ophthalmol., 25, 123–129, 1980.
Datta, S. and Banerjee, D. P.: Chorioretinitis in congenital toxoplasmosis, Indian Pediatr., 40, 790–791, 2003.
Davidson, M. G., and SR, N.: Disease of the lens and cataract formation, in: Vet Ophthalmol, edited by: KN Gelatt, Williams & Wilkins, Philadelphia, USA, 797–825, 1999.
Dielemans, I., Vingerling, J. R., Algra, D., Hofman, A., Grobbee, D. E., and de Jong, P. T.: Primary open-angle glaucoma, intraocular pressure, and systemic blood pressure in the general elderly population. The Rotterdam Study, Ophthalmology, 102, 54–60, 1995.
Dubicanac, M., Joly, M., Struve, J., Nolte, I., Mestre-Frances, N., Verdier, J. M., and Zimmermann, E.: Intraocular pressure in the smallest primate aging model: the gray mouse lemur, Vet. Ophthalmol., https://doi.org/10.1111/vop.12434, 2016.
Dubicanac, M., Struve, J., Mestre-Frances, N., Verdier, J. M., Zimmermann, E., and Joly, M.: Photoperiodic regime influences onset of lens opacities in a non-human primate, PeerJ., 5, e3258, https://doi.org/10.7717/peerj.3258, 2017.
Duy, T. P., Hoang, T. H., van den Bos, F., and Kenyon, M.: Successful cataract removal, and lens replacement on a rescued yellow-cheeked gibbon (Nomascus gabriellae), Vietnamese Journal of Primatology, 1, 69–74, 2010.
Eidsness, R. B., Stockl, F., and Colleaux, K. M.: West Nile chorioretinitis, Can. J. Ophthalmol., 40, 721–724, https://doi.org/10.1016/S0008-4182(05)80088-2, 2005.
Ennis, J., Burke, J., and Baxter, P.: Congenital corectopia (eccentric pupils): a marker for chromosomal and central nervous system abnormality, Eur. J. Paediatr. Neuro., 10, 27–29, https://doi.org/10.1016/j.ejpn.2005.09.002, 2006.
Faiq, M., Sharma, R., Dada, R., Mohanty, K., Saluja, D., and Dada, T.: Genetic, Biochemical and Clinical Insights into Primary Congenital Glaucoma, J. Curr. Glaucoma. Pract., 7, 66–84, https://doi.org/10.5005/jp-journals-10008-1140, 2013.
Ferreira, I. S., Bernardes, T. F., and Bonfioli, A. A.: Trichiasis, Semin. Ophthalmol., 25, 66–71, https://doi.org/10.3109/08820538.2010.488580, 2010.
Friedlaender, M. H. and Smolin, G.: Corneal degenerations, Ann. Ophthalmol., 11, 1485–1495, 1979.
Gao, Y., Li, W., Yin, Z., Ma, Y., Cai, H., and Tang, X.: Association between genetic polymorphisms of the beta adrenergic receptor and diurnal intraocular pressure in Chinese volunteers and glaucoma patients, Curr. Eye Res., 41, 1553–1560, https://doi.org/10.3109/02713683.2016.1139727, 2016.
Garcher, C., Bron, A., Bertrand, M. A., Chirpaz, L., and Bosc, J. M.: Ocular toxoplasmosis and AIDS. A case report, J. Fr. Ophtalmol., 13, 69–73, 1990.
Gelatt, K. N., Gilger, B. C., and Kern, T. J.: Veterinary Ophthalmology, 5th Edition, John Wiley & Sons, Chichester, UK, 2012.
Giugni, A. S., Mani, S., Kannan, S., and Hatipoglu, B.: Exophthalmos: a forgotten clinical sign of Cushing's Syndrome, Case Rep. Endocrinol., 2013, 205208, https://doi.org/10.1155/2013/205208, 2013.
Glover, T. D. and Constantinescu, G. M.: Surgery for cataracts, Vet. Clin. N. Am.-Small, 27, 1143–1173, 1997.
Gomez, D., Barbosa, A., Thery, M., Aujard, F., and Perret, M.: Age affects photoentrainment in a nocturnal primate, J. Biol. Rhythm., 27, 164–171, https://doi.org/10.1177/0748730411435223, 2012.
Griener, E. and Lambert, S. R.: Successful treatment of tractional corectopia using 2 mJ of energy with an Nd:YAG laser, J. Aapos., 3, 250–251, 1999.
Gump, D. W. and Holden, R. A.: Acquired chorioretinitis due to toxoplasmosis, Ann. Intern. Med., 90, 58–60, 1979.
Gwin, R. M. and Gelatt, K. N.: The canine lens, in: Vet Ophthalmol, edited by: Gelatt, K. N., John Wiley & Sons, Philadelphia, USA, 435–473, 1981.
Hafidi, Z. and Daoudi, R.: Inflammatory exophthalmos revealing an orbital hydatid cyst, Pan. Afr. Med. J., 15, 102, https://doi.org/10.11604/pamj.2013.15.102.3088, 2013.
Hall, B. R., Oliver, G. E., and Wilkinson, M.: A presentation of longstanding toxoplasmosis chorioretinitis, Optometry, 80, 23–28, https://doi.org/10.1016/j.optm.2008.03.007, 2009.
Hejtmancik, J. F. and Kantorow, M.: Molecular genetics of age-related cataract, Exp. Eye. Res., 79, 3–9, https://doi.org/10.1016/j.exer.2004.03.014, 2004.
Hilgert, C. R., Hilgert, G. L., Hardoim, V. A., and Omi, C. A.: Late recurrent iris synechia following laser goniopuncture for deep sclerectomy enhancement: case report, Arq. Bras. Oftalmol., 75, 433–435, 2012.
Jun Hu, Y. and Chen, W. Q.: Correspondence: the effects of two kinds of mydriatics on preventing postoperative posterior synechia, Retina, 30, p. 186, https://doi.org/10.1097/IAE.0b013e3181bd31f1, 2010.
Kaback, M., Scoper, S. V., Arzeno, G., James, J. E., Hua, S. Y., Salem, C., Dickerson, J. E., Landry, T. A., and Bergamini, M. V.: for the Brinzolamide 1 %/Timolol 0.5 % Study Group: Intraocular pressure-lowering efficacy of brinzolamide 1 %/timolol 0.5 % fixed combination compared with brinzolamide 1 % and timolol 0.5 %, Ophthalmology, 115, 1728–1734, https://doi.org/10.1016/j.ophtha.2008.04.011, 2008.
Kass, M. A., Heuer, D. K., Higginbotham, E. J., Johnson, C. A., Keltner, J. L., Miller, J. P., Parrish, R. K., 2nd, Wilson, M. R., and Gordon, M. O.: The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma, Arch. Ophthalmol., 120, 701–713, 2002.
Keil, S. and Davidson, H.: FEATURES-Canine cataracts: a review of diagnostic and treatment procedures–thousands of dogs develop cataracts every year. Though you may not personally perform cataract surgery, you should be, Vet. Med.-Us., 96, 14–38, 2001.
Kim, S. W., Oh, J., Song, J. S., Kim, Y. Y., Oh, I. K., and Huh, K.: Risk factors of iris posterior synechia formation after phacovitrectomy with three-piece acrylic IOL or single-piece acrylic IOL, Ophthalmologica, 223, 222–227, https://doi.org/10.1159/000203366, 2009.
Kinshuck, D.: Glauline (metipranolol) induced uveitis and increase in intraocular pressure, Brit. J. Ophthalmol., 75, 575–575, https://doi.org/10.1136/bjo.75.9.575, 1991.
Kirk, E. C.: Comparative morphology of the eye in primates, Anat. Rec. Part. A, 281, 1095–1103, https://doi.org/10.1002/ar.a.20115, 2004.
Kirkwood, B. J. and Kirkwood, R. A.: Trichiasis: characteristics and management options, Insight, 36, 5–9, 2011.
Klein, A. P., Duggal, P., Lee, K. E., O'Neill, J. A., Klein, R., Bailey-Wilson, J. E., and Klein, B. E.: Polygenic effects and cigarette smoking account for a portion of the familial aggregation of nuclear sclerosis, Am. J. Epidemiol., 161, 707–713, https://doi.org/10.1093/aje/kwi102, 2005a.
Klein, B. E.: Lens opacities in women in Beaver Dam, Wisconsin: is there evidence of an effect of sex hormones?, T. Am. Ophthal. Soc., 91, 517–544, 1993.
Klein, B. E., Klein, R., and Knudtson, M. D.: Intraocular pressure and systemic blood pressure: longitudinal perspective: the Beaver Dam Eye Study, Brit. J. Ophthalmol., 89, 284–287, https://doi.org/10.1136/bjo.2004.048710, 2005b.
Klein, B. E., Klein, R., and Linton, K. L.: Prevalence of age-related lens opacities in a population. The Beaver Dam Eye Study, Ophthalmology, 99, 546–552, 1992.
Klintworth, G. K.: Corneal dystrophies, Orphanet. J. Rare. Dis., 4, 7, https://doi.org/10.1186/1750-1172-4-7, 2009.
Koehler, M. P. and Sholiton, D. B.: Spontaneous hyphema resulting from warfarin, Ann. Ophthalmol., 15, 858–859, 1983.
van Koolwijk, L. M., Despriet, D. D., van Duijn, C. M., Pardo Cortes, L. M., Vingerling, J. R., Aulchenko, Y. S., Oostra, B. A., Klaver, C. C., and Lemij, H. G.: Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology, Invest. Ophth. Vis. Sci., 48, 3669–3676, https://doi.org/10.1167/iovs.06-1519, 2007.
van Koolwijk, L. M., Ramdas, W. D., Ikram, M. K., Jansonius, N. M., Pasutto, F., Hysi, P. G., Macgregor, S., Janssen, S. F., Hewitt, A. W., Viswanathan, A. C., ten Brink, J. B., Hosseini, S. M., Amin, N., Despriet, D. D., Willemse-Assink, J. J., Kramer, R., Rivadeneira, F., Struchalin, M., Aulchenko, Y. S., Weisschuh, N., Zenkel, M., Mardin, C. Y., Gramer, E., Welge-Lussen, U., Montgomery, G. W., Carbonaro, F., Young, T. L., The DCCT/EDIC Research Group, Bellenguez, C., McGuffin, P., Foster, P. J., Topouzis, F., Mitchell, P., Wang, J. J., Wong, T. Y., Czudowska, M. A., Hofman, A., Uitterlinden, A. G., Wolfs, R. C., de Jong, P. T., Oostra, B. A., Paterson, A. D., Wellcome Trust Case Control Consortium, Mackey, D. A., Bergen, A. A., Reis, A., Hammond, C. J., Vingerling, J. R., Lemij, H. G., Klaver, C. C., and van Duijn, C. M.: Common genetic determinants of intraocular pressure and primary open-angle glaucoma, PLoS Genet., 8, e1002611, https://doi.org/10.1371/journal.pgen.1002611, 2012.
Kumar, V., Robinson, R., and Ainsworth, J. R.: Idiopathic tractional corectopia, Brit. J. Ophthalmol., 84, 1206–1206, 2000.
Languille, S., Blanc, S., Blin, O., Canale, C. I., Dal-Pan, A., Devau, G., Dhenain, M., Dorieux, O., Epelbaum, J., Gomez, D., Hardy, I., Henry, P. Y., Irving, E. A., Marchal, J., Mestre-Frances, N., Perret, M., Picq, J. L., Pifferi, F., Rahman, A., Schenker, E., Terrien, J., Thery, M., Verdier, J. M., and Aujard, F.: The grey mouse lemur: a non-human primate model for ageing studies, Ageing Res. Rev., 11, 150–162, https://doi.org/10.1016/j.arr.2011.07.001, 2012.
Leske, M. C., Wu, S. Y., Nemesure, B., Hennis, A., and Barbados Eye Studies G: Risk factors for incident nuclear opacities, Ophthalmology, 109, 1303–1308, 2002.
Maggs, D. J., Miller, P., and Ofri, R.: Slatter's Fundamentals of Veterinary Ophthalmology, Elsevier Health Sciences, St Louis, Missouri, USA, 2012.
Manousaridis, K., Reichart-Peter, S., and Mennel, S.: Orbital emphysema with exophthalmos following transconjunctival pars plana vitrectomy, Ophthalmologe, 114, 734–736, https://doi.org/10.1007/s00347-016-0364-z, 2016.
McDonald, C. J., Raafat, A., Mills, M. J., and Rumble, J. A.: Medical and surgical management of spontaneous hyphaema secondary to immune thrombocytopenia, Brit. J. Ophthalmol., 73, 922–925, 1989.
Menezo, J. L. and Illueca, A.: Vitrectomy for intraocular foreign bodies and their complications, J. Fr. Ophtalmol., 6, 135–138, 1983.
Michael, R. and Bron, A. J.: The ageing lens and cataract: a model of normal and pathological ageing, Philos. T. Roy. Soc. B, 366, 1278–1292, https://doi.org/10.1098/rstb.2010.0300, 2011.
Milea, D. and Burillon, C.: Excimer laser photorefractive keratectomy in myopic eyes with corectopia, J. Cataract. Refr. Surg., 25, 709–711, 1999.
Mitchell, N.: Ophthalmology: hyphaema in dogs, Companion Animal, 11, 85–89, https://doi.org/10.1111/j.2044-3862.2006.tb00514.x, 2006.
Mittermeier, R., Louis, J. E., Richardson, M., Schwitzer, C., Langrand, O., Rylands, A., Hawkins,F., Rajaobelina, S., Ratsimbazafy, J., Rasoloarison, R., Roos, C., Kappeler, P., and Mackinnon, J.: Lemurs of Madagascar, Conservation International, Washington, DC, 2010.
Moffat, B. A., Landman, K. A., Truscott, R. J., Sweeney, M. H., and Pope, J. M.: Age-related changes in the kinetics of water transport in normal human lenses, Exp. Eye. Res., 69, 663–669, https://doi.org/10.1006/exer.1999.0747, 1999.
Molina-Socola, F. E., Lopez-Herrero, F., Medina-Tapia, A., Rueda-Rueda, T., Contreras-Diaz, M., and Sanchez-Vicente, J. L.: Syphilitic posterior placoid chorioretinitis as initial presentation of early neurosyphilis, Arch. Soc. Esp. Oftalmol., 92, 490–494, https://doi.org/10.1016/j.oftal.2016.10.019, 2016.
Montoya, J. G. and Remington, J. S.: Toxoplasmic chorioretinitis in the setting of acute acquired toxoplasmosis, Clin. Infect. Dis., 23, 277–282, 1996.
Morax, S. and Badelon, I.: Basedow exophthalmos, J. Fr. Ophtalmol., 32, 589–599, https://doi.org/10.1016/j.jfo.2009.09.001, 2009.
Ohrstrom, A.: Treatment of traumatic hyphaema with corticosteroids and mydriatics, Acta Ophthalmol., 50, 549–555, 1972.
Ornek, K., Buyuktortop, N., Ornek, N., Ogurel, R., Erbahceci, I. E., and Onaran, Z.: Effect of 1 % brinzolamide and 0.5 % timolol fixed combination on intraocular pressure after cataract surgery with phacoemulsification, Int. J. Ophthalmol., 6, 851–854, https://doi.org/10.3980/j.issn.2222-3959.2013.06.19, 2013.
Pandolfi, M., Nilsson, I. M., and Nilehn, J. E.: On intraocular fibrinolysis, Thromb. Diath. Haemost., 15, 161–172, 1966.
Perret, M.: Change in photoperiodic cycle affects life span in a prosimian primate (Microcebus murinus), J. Biol. Rhythm., 12, 136–145, 1997.
Psilas, K., Petroutsos, G., and Aspiotis, M.: Treatment of toxoplasmosis. The treatment of toxoplasmic chorioretinitis, J. Fr. Ophtalmol., 13, 551–553, 1990.
Radcliffe, N. M. and Finger, P. T.: Eye cancer related glaucoma: current concepts, Surv. Ophthalmol., 54, 47–73, https://doi.org/10.1016/j.survophthal.2008.10.002, 2009.
Rakusin, W.: Traumatic hyphema, Am. J. Ophthalmol., 74, 284–292, 1972.
Read, J. and Goldberg, M.: Comparison of medical treatment for traumatic hyphema, T. Am. Acad. Ophthalmol., 78, 799–815, 1974.
Ross, C. F. and Kirk, E. C.: Evolution of eye size and shape in primates, J. Hum. Evol., 52, 294–313, https://doi.org/10.1016/j.jhevol.2006.09.006, 2007.
Roszkowska, A. M. and Wylegala, E.: Corneal Degenerations, in: Studies on the Cornea and Lens, edited by: Babizhayev, A. M., Wan-Cheng Li, D., Kasus-Jacobi, A., Žorić L., and Alió J. L., Springer, New York, USA, 23–38, 2015.
Rowsey, J. J. and Gaylor, J. R.: Intraocular lens disasters: peripheral anterior synechia, Ophthalmology, 87, 646–664, 1980.
Sacca, S. C., Roszkowska, A. M., and Izzotti, A.: Environmental light and endogenous antioxidants as the main determinants of non-cancer ocular diseases, Mutat. Res., 752, 153–171, https://doi.org/10.1016/j.mrrev.2013.01.001, 2013.
Sandhu, S., Arora, S., and Edwards, M. C.: A case of delayed-onset recurrent hyphema after iStent surgery, Can. J. Ophthalmol., 51, e165–e167, https://doi.org/10.1016/j.jcjo.2016.07.001, 2016.
Sato, T.: A new proposal for the surgical treatment of anterior synechia, Am. J. Ophthalmol., 36, 698–704, 1953.
Schiff, F. S.: Coumadin related spontaneous hyphemas in patients with iris fixated pseudophakos, Ophthalmic Surg., 16, 172–173, 1985.
Shields, C. L., Materin, M. A., Shields, J. A., Gershenbaum, E., Singh, A. D., and Smith, A.: Factors associated with elevated intraocular pressure in eyes with iris melanoma, Brit. J. Ophthalmol., 85, 666–669, 2001.
Shiose, Y.: Intraocular pressure: new perspectives, Surv. Ophthalmol., 34, 413–435, 1990.
Soares, Í. P., and França, V. P.: Evisceration and enucleation, Semin. Ophthalmol., 25, 94–97, https://doi.org/10.3109/08820538.2010.488575, 2010.
Sourdille, G. P.: Treatment of iris impaction and synechia after operation of cataract, Bull. Soc. Ophtalmol. Fr., 5, 460–463, 1954.
Speakman, J. S.: Recurrent hyphema after surgery, Can. J. Ophthalmol., 10, 299–304, 1975.
Swan, K. C.: Hyphema due to wound vascularization after cataract extraction, Arch. Ophthalmol., 89, 87–90, 1973.
Sweeney, M. H. and Truscott, R. J.: An impediment to glutathione diffusion in older normal human lenses: a possible precondition for nuclear cataract, Exp. Eye. Res., 67, 587–595, https://doi.org/10.1006/exer.1998.0549, 1998.
Takeuchi, M., Kanda, T., Taguchi, M., Shibata, M., Mine, I., and Sakurai, Y.: Evaluation of efficacy and safety of latanoprost/timolol vs. travoprost/timolol fixed combinations for ocular hypertension associated with uveitis, Ocul. Immunol. Inflamm., 25, 105–110, https://doi.org/10.3109/09273948.2015.1092559, 2017.
Telle, M. R. and Betbeze, C.: Hyphema: considerations in the Small Animal Patient, Top. Companion. Anim. M., 30, 97–106, https://doi.org/10.1053/j.tcam.2015.07.008, 2015.
Thylefors, B., Chylack, L. T., Jr., Konyama, K., Sasaki, K., Sperduto, R., Taylor, H. R., West, S., and Group, W. H. O. C. G.: A simplified cataract grading system, Ophthalmic. Epidemiol., 9, 83–95, 2002.
Truscott, R. J.: Age-related nuclear cataract-oxidation is the key, Exp. Eye. Res., 80, 709–725, https://doi.org/10.1016/j.exer.2004.12.007, 2005.
Vardarli, M. C., Mokan, P., Hupfer, U., Gerressen, M., Hansch, A., Schierle, K., Boicev, A. D., and Kohler, T. K.: Unilateral gigantic exophthalmos in haemorrhagic exacerbation of an orbital meningioma, Klin. Monatsbl. Augenh., 233, 965–966, https://doi.org/10.1055/s-0042-108652, 2016.
Verdier, J. M., Acquatella, I., Lautier, C., Devau, G., Trouche, S., Lasbleiz, C., and Mestre-Frances, N.: Lessons from the analysis of nonhuman primates for understanding human aging and neurodegenerative diseases, Front Neurosci., 9, 64, https://doi.org/10.3389/fnins.2015.00064, 2015.
Weigl, R. and Jones, M.: Longevity of Mammals in Captivity: from the Living Collections of the World: a List of Mammalian Longevity in Captivity, Schweizerbart, Stuttgart, Germany, 2005.
Weiss, J. S., Moller, H. U., Lisch, W., Kinoshita, S., Aldave, A. J., Belin, M. W., Kivela, T., Busin, M., Munier, F. L., Seitz, B., Sutphin, J., Bredrup, C., Mannis, M. J., Rapuano, C. J., Van Rij, G., Kim, E. K., and Klintworth, G. K.: The IC3D classification of the corneal dystrophies, Cornea, 27, S1–83, https://doi.org/10.1097/ICO.0b013e31817780fb, 2008.
Weiss, J. S., Moller, H. U., Aldave, A. J., Seitz, B., Bredrup, C., Kivela, T., Munier, F. L., Rapuano, C. J., Nischal, K. K., Kim, E. K., Sutphin, J., Busin, M., Labbe, A., Kenyon, K. R., Kinoshita, S., and Lisch, W.: IC3D classification of corneal dystrophies–edition 2, Cornea, 34, 117–159, https://doi.org/10.1097/ICO.0000000000000307, 2015.
Werner, S. C.: Classification of the eye changes of Grave's disease, J. Clin. Endocr. Metab., 29, 982–984, https://doi.org/10.1210/jcem-29-7-982, 1969.
Wilkie, D. A. and Colitz, C. M.: Update on veterinary cataract surgery, Curr. Opin. Ophthalmol., 20, 61–68, https://doi.org/10.1097/ICU.0b013e32831a98aa, 2009.
Williams, D. L. and Kim, J. Y.: Feline entropion: a case series of 50 affected animals (2003–2008), Vet. Ophthalmol., 12, 221–226, https://doi.org/10.1111/j.1463-5224.2009.00705.x, 2009.
Yang, B., Xiao, J., Li, X., Luo, L., Tong, B., and Su, G.: Clinical manifestations of syphilitic chorioretinitis: a retrospective study, Int. J. Clin. Exp. Med., 8, 4647–4655, 2015.
Yasuna, E.: Management of traumatic hyphema, Arch. Ophthalmol., 91, 190–191, 1974.
Zimmermann, E. and Radespiel, U.: Species concepts, diversity, and evolution in primates: lessons to be learned from mouse lemurs, Evol. Anthropol., 23, 11–14, https://doi.org/10.1002/evan.21388, 2014.
Zimmermann, E. and Radespiel, U.: Handbook of Paleoanthropology, Springer, NY, USA, 2015.
Zimmermann, E., Radespiel, U., Mestre-Francés N., and Verdier, J. M.: Life history variation in mouse lemurs (Microcebus murinus, M. lehilahytsara): phylogenetic determinants, in: The Dwarf and Mouse Lemurs of Madagascar: Biology, Behavior and Conservation Biogeography of the Cheirogaleidae, edited by: Lehmann, S. M., Radespiel, U., and Zimmermann, E., Cambridge University Press, Cambridge, 174–194, 2016.
Short summary
This review shows that mouse lemurs show various ocular impairments which may distort vision. The most widespread and obvious ocular finding were nuclear sclerosis and cataracts. Both highly increase with increasing age. Iris posterior synechia has been described in different colonies and seems highly age dependent and cataract associated. Combined with the variety of many other eye diseases, special ophthalmological treatments and examinations are required to ensure animal well-being.
This review shows that mouse lemurs show various ocular impairments which may distort vision....