Ocular Pigmentation in White and Siamese Cats

Total Page:16

File Type:pdf, Size:1020Kb

Ocular Pigmentation in White and Siamese Cats Ocular pigmentation in white and Siamese cats L. N. Thibos, W. R. Levick, and R. Morstyn Ocular pigmentation in white cats with blue and. yellow eyes and in Siamese cats was examined ophthalmoscopically and histologically. Yellow-eyed, white cats had. entirely normal ocular pigmentation. Blue eyes of white cats had. normal pigmentation of the iridial and. retinal pigment epithelia but no stromal pigmentation of the iris or choroid. This deficit is apparently due to the absence of stromal pigment cells, certainly in the iris. As a general rule, the blue eye of white cats had no tapetum. Siamese cats had reduced pigmentation of the iridial and retinal pigment epithelia and no stromal pigmentation of the iris or choroid. The lack of pigmentation is apparently due to the inability of stromal pigment cells to produce pigment, certainly in the iris. We conclude that the abnormality of visual pathways previously described, in the Siamese cat is not due simply to a deficiency of pigment in cells of neural crest origin. Key words: ocular pigments, white cats, Siamese cats, iris pigment, choroid pigment v3iamese and white cats are two breeds This report describes the extent of ocular which have a deficiency of coat pigmentation pigmentation in white cats as compared with and which can also have reduced ocular pig- Siamese and normally pigmented cats. Sev- mentation. The comparative details of this eral of the animals used in these experiments hypopigmentation are of interest because the were also subjects in neurophysiological in- Siamese cat suffers from an abnormal visual vestigations of the visual pathways which are 1 3 4 pathway " yet the white cat does not. Al- described elsewhere.4 bino individuals of other mammalian species have pathway abnormalities similar to those Methods in the Siamese cat, and the suggestion has Ophthalmoscopic observations of six adult white been made that the cause might be specifical- cats (A through F) of undetermined genetic con- ly related to the amount of pigment in the stitution were made after each animal was pre- retinal epithelium.5' 6 pared for neurophysiological recordings. The pupil was dilated with atropine drops (1%), and a zero-power contact lens was fitted. Additional ob- servations were made on six white, five Siamese, From the Department of Physiology, John Curtin School and one solid black cat (cats G through S). Color of Medical Research, Australian National University, photographs of the fundus and iris were taken with Canberra, Australia. a Zeiss fundus camera and Kodacolor 400 film. L. N. Thibos was supported by a Postdoctoral Fellow- Upon completion of neurophysiological exper- ship of the U. S. Public Health Service. R. Morstyn iments, a dose of about 30 mg of pentobarbitone was a Vacation Scholar of the Australian National Uni- per kilogram of body weight was administered in- versity. Submitted for publication Dec. 27, 1978. travenously, and the eyes were enucleated. Each Reprint requests: Dr. W. R. Levick, Department of eye was then hemisected at the pars plana, the Physiology, John Curtin School of Medical Research, vitreous and lens were discarded, and the remain- Australian National University, P.O. Box 334, Can- der was fixed in 10% neutral buffered formal berra City, A.C.T. 2601, Australia. saline. 0146-0404/80/050475+12$01.20/0 © 1980 Assoc. for Res. in Vis. and Ophthal., Inc. 475 Downloaded from jov.arvojournals.org on 10/01/2021 Invest. Ophthalmol, Vis. Set. 476 Thibos, Levick, and Morstyn May 1980 Fig. 1. For legend see facing page. Downloaded from jov.arvojournals.org on 10/01/2021 Volume 19 Number 5 Ocular pigmentation in cat All To get satisfactory iris preparations, animals G illumination the iris had a translucent to di- through R, which were not part of neurophysiolog- aphanous appearance, quite different in side- ical experiments, were given 2 drops of 0.5% by-side comparison with irides of white cats. physostigmine to contract the pupil. A lethal dose Fundus. The dominant feature of an ordi- of pentobarbitone was administered, and the eyes nary pigmented cat's fundus is the yellow- were enucleated and fixed as described above. green tapetum which is surrounded by very Before the histological preparation was begun, fundus tissue was sandwiched between slices of dark pigmentation. Although the precise size and shape of the tapetum varies somewhat fixed cat liver to minimize detachment of the ret- 7 ina from the choroid. Tissues were embedded in from cat to cat, it is possible to predict the paraffin, and 5 /u,m sections were prepared with location of the tapetum with acceptable reli- hematoxylin and eosin stain. In some preparations ability. We shall refer to this fiducial region melanin pigment was bleached by treatment with where one expects to find a tapetal reflection 0.1% potassium permanganate followed by 1% as the tapetal zone. The statements which oxalic acid. Photomicrographs were taken with a follow are based upon complete ophthalmo- Zeiss photomicroscope. scopic and microdissection surveys of the entire fundi supported by selected fundus Results photographs. Ophthalmoscopic and microdissection ob- The fundi of yellow-eyed white cats had servations. A summary of the gross appear- the same appearance as those of ordinary ance of the irides and fundi of the 18 subjects pigmented cats. A yellow-green reflection is given in Table I. from the tapetal zone and the retinal blood Iris. Color photographs of the living cat iris vessels within this region were clearly visible are given in Fig. 1, A, for a yellow-eyed ophthalmoscopically (e.g., upper part of Fig. white cat and in Fig. 1, C, for a blue-eyed 1, B). The shape and size of the tapetum was white cat. Dissection of the eyes of white cats within the normal range.7 The nontapetal revealed the posterior surfaces of the irides to zone appeared dark brown (e.g., lower part be as darkly pigmented as in the ordinary of Fig. 1, B) due to the presence of pigment pigmented cat. Side-by-side comparison un- in both the retinal epithelium and choroid as der transillumination showed that the yellow observed by microdissection. However, in and blue irides of white cats were each as eight of 12 eyes there were horizontally elon- opaque as the yellow iris of a black cat. gated patches of inferior fundus about 5 to The blue iris of a seal-point Siamese cat is 10 mm wide and 2 to 4 mm high where shown in Fig. 1, E. The posterior surface of choroidal pigment was completely missing. the Siamese iris was not as heavily pigmented Apart from these patches, the choroid was as in the ordinary pigmented cat, appearing a equally heavily pigmented inside and outside dark chocolate brown in the seal point and a the tapetal zone. lighter brown in the lilac point. Under trans- The fundus of the usual blue-eyed white Fig. 1. Iris and fundus of the living cat eye. Shown are yellow-eyed white cat iris (A) and fundus (B), blue-eyed white cat iris (C) and fundus (D), and seal-point Siamese iris (E) and fundus (F) (left eye of animals Q, R, and S, respectively). The darkly pigmented pupillary ruff of the epithelium, located at the pupil margin, is more evident in A and C than in E. Note the translucent quality of the Siamese iris. Fundus photographs all show the inferior border of the tapetal zone with the retinal blood vessels exiting from the optic nerve head in the upper left of the picture. Each field subtends about 30° of visual angle and each is centered approximately 15° below and 7° nasal to the center of the area centralis, so as to show parts of both tapetal and nontapetal zones. B has the appearance of the ordinary pigmented cat's fundus. D lacks both tapetum and choroidal pigment, thereby revealing choroidal blood vessels. Clumps of retinal epithelial pigment are evident at the bottom of D. Because of the absence of a reflecting tapetum, the exposure for this photograph had to be increased substantially relative to B and F. F has a tapetum, dilute epithelial pigment, but no choroidal pigment; thus the choroidal vessels are visible below the tapetal zone. Downloaded from jov.arvojournals.org on 10/01/2021 Invest. Ophthalmol. Vis. Sci. 478 Thibos, Levick, and Morstyn May 1980 Table I. Summary of macroscopic appearance of ocular pigmentation Cat identification /breed G A F H Q B D E L C I p R J M N s K Eye Bl W W W w W W W W W w- w W SS SS SS SS LS Iris color Y Y By Y By B B B B B B B B R Y Y Y Y Bv B B B B B B B B B Iris epithelium L 0 o o o o R o 0 o o o Choroid L Of o o o 0 o o o o R o o o o o o o o o Tapetum L O o o o R o o o o Retina epithelium L O G O O O outside tapetal zone R O O O O O W = white cat; Bl = black cat; SS = Seal-point Siamese cat; LS = Lilac-point Siamese cat. Letter O not used for identification of cat. Y = yellow appearance; B = blue appearance; By = blue with yellow sector. Key: • Pigment (or tapetum) present; O pigment diluted; O pigment (or tapetum) absent. '"Absence of pigment in a portion of inferior fundus. tQuadrantic sector of pigment in temporal midperiphery. cat was strikingly different from that of the same as for the white cats described above.
Recommended publications
  • 12 Retina Gabriele K
    299 12 Retina Gabriele K. Lang and Gerhard K. Lang 12.1 Basic Knowledge The retina is the innermost of three successive layers of the globe. It comprises two parts: ❖ A photoreceptive part (pars optica retinae), comprising the first nine of the 10 layers listed below. ❖ A nonreceptive part (pars caeca retinae) forming the epithelium of the cil- iary body and iris. The pars optica retinae merges with the pars ceca retinae at the ora serrata. Embryology: The retina develops from a diverticulum of the forebrain (proen- cephalon). Optic vesicles develop which then invaginate to form a double- walled bowl, the optic cup. The outer wall becomes the pigment epithelium, and the inner wall later differentiates into the nine layers of the retina. The retina remains linked to the forebrain throughout life through a structure known as the retinohypothalamic tract. Thickness of the retina (Fig. 12.1) Layers of the retina: Moving inward along the path of incident light, the individual layers of the retina are as follows (Fig. 12.2): 1. Inner limiting membrane (glial cell fibers separating the retina from the vitreous body). 2. Layer of optic nerve fibers (axons of the third neuron). 3. Layer of ganglion cells (cell nuclei of the multipolar ganglion cells of the third neuron; “data acquisition system”). 4. Inner plexiform layer (synapses between the axons of the second neuron and dendrites of the third neuron). 5. Inner nuclear layer (cell nuclei of the bipolar nerve cells of the second neuron, horizontal cells, and amacrine cells). 6. Outer plexiform layer (synapses between the axons of the first neuron and dendrites of the second neuron).
    [Show full text]
  • Morphological Aspect of Tapetum Lucidum at Some Domestic Animals
    Bulletin UASVM, Veterinary Medicine 65(2)/2008 pISSN 1843-5270; eISSN 1843-5378 MORPHOLOGICAL ASPECT OF TAPETUM LUCIDUM AT SOME DOMESTIC ANIMALS Donis ă Alina, A. Muste, F.Beteg, Roxana Briciu University of Angronomical Sciences and Veterinary Medicine Calea M ănăş tur 3-5 Cluj-Napoca [email protected] Keywords: animal ophthalmology, eye fundus, tapetum lucidum. Abstract: The ocular microanatomy of a nocturnal and a diurnal eye are very different, with compromises needed in the arrhythmic eye. Anatomic differences in light gathering are found in the organization of the retina and the optical system. The presence of a tapetum lucidum influences the light. The tapetum lucidum represents a remarkable example of neural cell and tissue specialization as an adaptation to a dim light environment and, despite these differences, all tapetal variants act to increase retinal sensitivity by reflecting light back through the photoreceptor layer. This study propose an eye fundus examination, in animals of different species: cattles, sheep, pigs, dogs cats and rabbits, to determine the presence or absence of tapetum lucidum, and his characteristics by species to species, age and even breed. Our observation were made between 2005 - 2007 at the surgery pathology clinic from FMV Cluj, on 31 subjects from different species like horses, dogs and cats (25 animals). MATERIAL AND METHOD Our observation were made between 2005 - 2007 at the surgery pathology clinic from FMV Cluj, on 30 subjects from different species like cattles, sheep, pigs, dogs cats and rabbits.The animals were halt and the examination was made with minimal tranquilization. For the purpose we used indirect ophthalmoscopy method with indirect ophthalmoscope Heine Omega 2C.
    [Show full text]
  • Characteristics of Structures and Lesions of the Eye in Laboratory Animals Used in Toxicity Studies
    J Toxicol Pathol 2015; 28: 181–188 Concise Review Characteristics of structures and lesions of the eye in laboratory animals used in toxicity studies Kazumoto Shibuya1*, Masayuki Tomohiro2, Shoji Sasaki3, and Seiji Otake4 1 Testing Department, Nippon Institute for Biological Science, 9-2221-1 Shin-machi, Ome, Tokyo 198-0024, Japan 2 Clinical & Regulatory Affairs, Alcon Japan Ltd., Toranomon Hills Mori Tower, 1-23-1 Toranomon, Minato-ku, Tokyo 105-6333, Japan 3 Japan Development, AbbVie GK, 3-5-27 Mita, Minato-ku, Tokyo 108-6302, Japan 4 Safety Assessment Department, LSI Medience Corporation, 14-1 Sunayama, Kamisu-shi, Ibaraki 314-0255, Japan Abstract: Histopathology of the eye is an essential part of ocular toxicity evaluation. There are structural variations of the eye among several laboratory animals commonly used in toxicity studies, and many cases of ocular lesions in these animals are related to anatomi- cal and physiological characteristics of the eye. Since albino rats have no melanin in the eye, findings of the fundus can be observed clearly by ophthalmoscopy. Retinal atrophy is observed as a hyper-reflective lesion in the fundus and is usually observed as degenera- tion of the retina in histopathology. Albino rats are sensitive to light, and light-induced retinal degeneration is commonly observed because there is no melanin in the eye. Therefore, it is important to differentiate the causes of retinal degeneration because the lesion occurs spontaneously and is induced by several drugs or by lighting. In dogs, the tapetum lucidum, a multilayered reflective tissue of the choroid, is one of unique structures of the eye.
    [Show full text]
  • Microscopic Anatomy of the Eye Dog Cat Horse Rabbit Monkey Richard R Dubielzig Mammalian Globes Mammalian Phylogeny General Anatomy Dog
    Microscopic Anatomy of the eye Dog Cat Horse Rabbit Monkey Richard R Dubielzig Mammalian globes Mammalian Phylogeny General Anatomy Dog Arterial Blood Vessels of the Orbit General Anatomy Dog * Horizontal section Long Posterior Ciliary a. Blood enters the globe Short Post. Ciliary a Long Post. Ciliary a. Anterior Ciliary a. Blood Supply General Anatomy Dog Major arterial circle of the iris Orbital Anatomy Dog Brain Levator Dorsal rectus Ventral rectus Zygomatic Lymph node Orbital Anatomy Dog Orbital Anatomy Dog Cartilaginous trochlea and the tendon of the dorsal oblique m. Orbital Anatomy Dog Rabbit Orbital Anatomy Dog Zygomatic salivary gland mucinous gland Orbital Anatomy Dog Gland of the Third Eyelid Eye lids (dog) Eye lids (dog) Meibomian glands at the lid margin Holocrine secretion Eye lids (primate) Upper tarsal plate Lower tarsal plate Eye lids (rabbit) The Globe The Globe Dog Cat Orangutan Diurnal Horse Diurnal Cornea Epithelium Stromal lamellae Bowman’s layer Dolphin Descemet’s m Endothelium TEM of surface epithelium Cornea Doubling of Descemet’s Vimentin + endothelium Iris Walls: The vertebrate eye Iris Sphincter m. Dilator m Blue-eye, GFAP stain Iris Collagen Iris Cat Sphinctor m. Dilator m. Iris Cat Phyomelanocytes Iris Equine Corpora nigra (Granula iridica) seen in ungulates living without shade Ciliary body Pars plicata Ciliary muscle Pars plana Ciliary body Zonular ligaments Ciliary body Primarily made of fibrillin A major component of elastin Ciliary body Alcian Blue staining acid mucopolysaccharides: Hyaluronic acid Ciliary
    [Show full text]
  • Ophthalmology Abbreviations Alphabetical
    COMMON OPHTHALMOLOGY ABBREVIATIONS Listed as one of America’s Illinois Eye and Ear Infi rmary Best Hospitals for Ophthalmology UIC Department of Ophthalmology & Visual Sciences by U.S.News & World Report Commonly Used Ophthalmology Abbreviations Alphabetical A POCKET GUIDE FOR RESIDENTS Compiled by: Bryan Kim, MD COMMON OPHTHALMOLOGY ABBREVIATIONS A/C or AC anterior chamber Anterior chamber Dilators (red top); A1% atropine 1% education The Department of Ophthalmology accepts six residents Drops/Meds to its program each year, making it one of nation’s largest programs. We are anterior cortical changes/ ACC Lens: Diagnoses/findings also one of the most competitive with well over 600 applicants annually, of cataract whom 84 are granted interviews. Our selection standards are among the Glaucoma: Diagnoses/ highest. Our incoming residents graduated from prestigious medical schools ACG angle closure glaucoma including Brown, Northwestern, MIT, Cornell, University of Michigan, and findings University of Southern California. GPA’s are typically 4.0 and board scores anterior chamber intraocular ACIOL Lens are rarely lower than the 95th percentile. Most applicants have research lens experience. In recent years our residents have gone on to prestigious fellowships at UC Davis, University of Chicago, Northwestern, University amount of plus reading of Iowa, Oregon Health Sciences University, Bascom Palmer, Duke, UCSF, Add power (for bifocal/progres- Refraction Emory, Wilmer Eye Institute, and UCLA. Our tradition of excellence in sives) ophthalmologic education is reflected in the leadership positions held by anterior ischemic optic Nerve/Neuro: Diagno- AION our alumni, who serve as chairs of ophthalmology departments, the dean neuropathy ses/findings of a leading medical school, and the director of the National Eye Institute.
    [Show full text]
  • Entoptic Phenomena and Reproducibility Ofcorneal Striae
    Br J Ophthalmol: first published as 10.1136/bjo.71.10.737 on 1 October 1987. Downloaded from British Journal of Ophthalmology, 1987, 71, 737-741 Entoptic phenomena and reproducibility of corneal striae following contact lens wear MURRAY H JOHNSON, C MONTAGUE RUBEN, AND DAVID M PERRIGIN From the Institutefor Contact Lens Research, University of Houston- University Park, 4901 Calhoun Road, Houston, Texas 77004, USA SUMMARY Vertical corneal striae distributed across the posterior cornea are one of the objective signs ofclinically unacceptable corneal swelling (>6%) resulting from contact lens wear. This study reports that corneal striae are repeatable both in configuration and location with different levels of hypoxia. In most instances entoptic phenomena result from the presence of these lines. The results suggest that the healthy, avascular, transparent cornea has certain localised areas in its anatomical structure which may give rise to bundles of collagen fibres being made visible objectively and subjectively during conditions of corneal swelling. Corneal striae is a term used to describe lines seen in vidual was strikingly similar. Furthermore, there was the corneal stroma of varied appearance, aetiology, intrasubject repeatability of striae with large inter- and pathology. Deep striae have been seen as a result subject variability of corneal striate lines. of trauma (penetrating wounds),' after intraocular In this paper we describe the repeatability and operations (striate keratitis),' in degenerative entoptic phenomena of corneal
    [Show full text]
  • Retinal Pigment Epithelial Lipofuscin and Melanin and Choroidal Melanin in Human Eyes
    Retinal Pigment Epithelial Lipofuscin and Melanin and Choroidal Melanin in Human Eyes John J. Weirer,*t Francois C. Delori,*t Glenn L. Wing,t and Karbrra A. Fitch* Optical measurements of the pigments of the retinal pigment epithelium (RPE) and choroid were made on 38 human autopsy eyes of both blacks and whites, varying in age between 2 wk and 90 yr old. Lipofuscin in melanin-bleached RPE was measured as fluorescence at 470 mm following excitation at 365 nm and was found to be proportional to fluorescence measured at 560 nm in unbleached tissue. Transmission measurements of RPE and choroidal melanin were converted and expressed as optical density units. The choroidal melanin content increased from the periphery to the posterior pole. RPE melanin concentration decreased from the periphery to the posterior pole with an increase in the macula. Conversely, the amount of RPE lipofuscin increased from the periphery to the posterior pole with a consistent dip at the fovea. There was an inverse relationship between RPE lipofuscin concentration and RPE melanin concentration. The RPE melanin content was similar between whites and blacks. Lipofuscin concentration was significantly greater (P = 0.002) in the RPE of whites compared to blacks; whereas blacks had a significantly greater (P = 0.005) choroidal melanin content than whites. The amounts of both choroidal and RPE melanin showed a trend of decreasing content with aging, whereas the amount RPE lipofuscin tended to increase (whites > blacks). Per fundus area, the amount of choroidal melanin was always greater than that in the RPE. There was a statistically significant (P = 0.001) increase in RPE height with age, most marked in eyes of whites after age 50 and correlated with the increase in lipofuscin concentration.
    [Show full text]
  • CORNEAL VASCULARIZATION in the FLORIDA MANATEE (Trichechus Manatus Latirostris)
    CORNEAL VASCULARIZATION IN THE FLORIDA MANATEE (Trichechus manatus latirostris) By JENNIFER YOUNG HARPER A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2004 Copyright 2004 by Jennifer Young Harper ACKNOWLEDGMENTS I would like to thank my mentor, Dr. Don Samuelson. He has been a wonderful source of knowledge, inspiration, and motivation. Without his help and guidance, I could not have accomplished any of this work. I would also like to thank Dr. Roger Reep for all of his help and support along the way. He too has acted as a rock and support system. My additional committee members (Dr. Peter McGuire, Dr. Dennis Brooks, and Dr. Gordon Bauer) have been tremendous support and I thank them for all they have offered. Their guidance has been appreciated beyond belief. Laboratory technologists Pat Lewis and Maggie Stoll were extremely helpful and supportive during much of my work. I would have not been able to accomplish the first procedure without their help. I thank these fine ladies from the bottom of my heart. My parents, Jim and Marion Young, have meant more to me than I can ever describe or explain. I appreciate all their love and support. Finally, I thank my husband Ridge Harper. He has been the strongest support system I could ever ask for and makes me happier than I ever knew I could be. iii TABLE OF CONTENTS page ACKNOWLEDGMENTS ................................................................................................
    [Show full text]
  • Microsporidial Stromal Keratitis
    CLINICOPATHOLOGIC REPORTS, CASE REPORTS, AND SMALL CASE SERIES SECTION EDITOR: W. RICHARD GREEN, MD Microsporidial Stromal Keratitis Microsporida are spore-forming, ob- ligate eukaryotic protozoan para- sites that belong to the phylum Microspora. The ophthalmic mani- festations of ocular microsporidi- osis exhibit characteristic clinical fea- tures depending on the genus involved. With the genus Encepha- Figure 1. The clinical appearance of the right Figure 2. The clinical appearance of the right litozoon, infection is limited to the cornea at the time of the initial examination cornea 9 months after the initial examination epithelial cells of the cornea and con- shows a central area of stromal infiltration and displays a central epithelial defect associated junctiva, producing a diffuse punc- edema without suppuration. A 3% hypopyon is with a disciform opacity. Superficial peripheral tate epithelial keratoconjunctivitis. present inferiorly. corneal vascularization is observed superiorly. With the genera Nosema and Micro- sporidium, the infection typically in- and scrapings collected for bacte- wrinkled and folded. The endothe- volves the corneal stroma, includ- rial, chlamydial, fungal, and herpes- lium was attenuated with a retro- ing the keratocytes.1 virus cultures were all negative for corneal fibrovascular membrane, To date, only 5 case reports of microorganisms. containing few neutrophils. The cor- microsporidial stromal keratitis have Over the next 2 months, the vi- neal stroma showed round to oval been published.2-6 We report an ad- sual acuity improved to 20/25 OD, organisms measuring 2.0 to 4.0 µm. ditional case caused by Vittaforma with gradual resolution of the stro- These organisms were mostly lo- corneae (formerly known as No- mal edema.
    [Show full text]
  • Funduscopic Interpretation Understanding the Fundus: Is That Normal?
    Funduscopic Interpretation Understanding the Fundus: is that normal? Gillian McLellan BVMS PhD DVOphthal DECVO DACVO MRCVS With thanks to Christine Heinrich and all who contributed images Fundus ≠ Retina working knowledge of fundus anatomy how to evaluate the fundus systematically normal fundus variants hallmarks of fundus pathology Fundus anatomy Vitreous normally optically clear (almost) Only retinal vessels / pigmented RPE +/- inner choroid (tapetum) make a major contribution to the typical appearance of a normal fundus Retinal Vascular Patterns holangiotic Retinal Vascular Patterns Merangiotic Paurangiotic Anangiotic Retinal anatomy light traverses 8 retinal layers to reach photoreceptor O.S. photoreceptors largely responsible for translucent appearance of NSR cone density highest in area centralis or macula RPE = single cell layer Pigmented /non-tapetal Tapetal / non-pigmented retinal anatomy tapetum structure within the choroid cellular in dog and cat regular compacted collagen array in ruminants, horses visible due to absence of pigment in overlying RPE seen ophthalmoscopically as a bright, shiny sweep of color (or not) Tapetal fundus Non-Tapetal fundus RPE Tapetal development RPE completely pigments during fetal development Autophagy of melanin occurs in presumptive tapetal zone RPE depigments Tapetal maturation is not complete until 12-14 weeks of age in dogs and cats Connecting capillaries In areas of thin tapetum choroidal vessels may segmentally shine through, in some cases the long posterior ciliary artery, or vortex veins may also be seen Tapetal variation in equine fundus Feline tapetum – transient variant Normal : Non-tapetal fundus Varies in color depending on amount of melanin in RPE and choroid RPE contains melanin, tapetum absent Normal : Non-tapetal fundus • non-tapetal fundus • (optic disc) • (retinal blood vessels) RPE contains melanin, where the tapetum is absent.
    [Show full text]
  • The Horizontal Raphe of the Human Retina and Its Watershed Zones
    vision Review The Horizontal Raphe of the Human Retina and its Watershed Zones Christian Albrecht May * and Paul Rutkowski Department of Anatomy, Medical Faculty Carl Gustav Carus, TU Dresden, 74, 01307 Dresden, Germany; [email protected] * Correspondence: [email protected] Received: 24 September 2019; Accepted: 6 November 2019; Published: 8 November 2019 Abstract: The horizontal raphe (HR) as a demarcation line dividing the retina and choroid into separate vascular hemispheres is well established, but its development has never been discussed in the context of new findings of the last decades. Although factors for axon guidance are established (e.g., slit-robo pathway, ephrin-protein-receptor pathway) they do not explain HR formation. Early morphological organization, too, fails to establish a HR. The development of the HR is most likely induced by the long posterior ciliary arteries which form a horizontal line prior to retinal organization. The maintenance might then be supported by several biochemical factors. The circulation separate superior and inferior vascular hemispheres communicates across the HR only through their anastomosing capillary beds resulting in watershed zones on either side of the HR. Visual field changes along the HR could clearly be demonstrated in vascular occlusive diseases affecting the optic nerve head, the retina or the choroid. The watershed zone of the HR is ideally protective for central visual acuity in vascular occlusive diseases but can lead to distinct pathological features. Keywords: anatomy; choroid; development; human; retina; vasculature 1. Introduction The horizontal raphe (HR) was first described in the early 1800s as a horizontal demarcation line that extends from the macula to the temporal Ora dividing the temporal retinal nerve fiber layer into a superior and inferior half [1].
    [Show full text]
  • Multimodal Imaging in a Patient with Prader–Willi Syndrome Mohamed A
    Hamid et al. Int J Retin Vitr (2018) 4:45 https://doi.org/10.1186/s40942-018-0147-6 International Journal of Retina and Vitreous CASE REPORT Open Access Multimodal imaging in a patient with Prader–Willi syndrome Mohamed A. Hamid*, Mitul C. Mehta and Baruch D. Kuppermann Abstract Background: Prader–Willi syndrome (PWS) is a genetic disease caused by loss of expression of the paternally inher- ited copy of several genes on the long arm of chromosome 15. Ophthalmic manifestations of PWS include strabismus, amblyopia, nystagmus, hypopigmentation of the iris and choroid, diabetic retinopathy, cataract and congenital ectro- pion uvea. An overlap between PWS and oculocutaneous albinism (OCA) has long been recognized and attributed to deletion of OCA2 gene located in PWS critical region (PWCR). Case report: A 30-year-old male patient with PWS presented with vision loss in his left eye. His right eye had normal visual acuity. Multimodal imaging revealed absence of a foveal depression and extremely reduced diameter of the foveal avascular zone in the right eye and an inactive type 2 macular neovascular lesion in the left eye. Conclusions: We report a presumed association of fovea plana and choroidal neovascularization with PWS. The use of multimodal imaging revealed novel fndings in a PWS patient that might enrich our current understanding of the overlap between PWS and OCA. Keywords: Prader–Willi syndrome, Fovea plana, Macular-foveal capillaries, Type 2 macular neovascularization Background stereopsis, amblyopia and nystagmus [1]. Hypopigmen- Prader–Willi syndrome (PWS) is a complex genetic tation of the iris and choroid, diabetic retinopathy, cata- disorder caused by lack of expression of the paternally- ract, congenital ocular fbrosis syndrome and congenital inherited PWS critical region (PWCR) of chromosome ectropion uvea have also been reported [3].
    [Show full text]