Analysis of the Variety of Eye Impairments in Glaucoma Cases in Children and Adults
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Case Report Descemet Stripping Endothelial Keratoplasty in a Patient with Keratoglobus and Chronic Hydrops Secondary to a Spontaneous Descemet Membrane Tear
Hindawi Publishing Corporation Case Reports in Ophthalmological Medicine Volume 2013, Article ID 697403, 5 pages http://dx.doi.org/10.1155/2013/697403 Case Report Descemet Stripping Endothelial Keratoplasty in a Patient with Keratoglobus and Chronic Hydrops Secondary to a Spontaneous Descemet Membrane Tear Anton M. Kolomeyer1 and David S. Chu1,2 1 The Institute of Ophthalmology and Visual Science, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark,NJ07103,USA 2 Metropolitan Eye Research and Surgery Institute, 540 Bergen Boulevard, Suite D, Palisades Park, NJ 07650, USA Correspondence should be addressed to David S. Chu; [email protected] Received 4 March 2013; Accepted 7 April 2013 Academic Editors: S. M. Johnson and S. Machida Copyright © 2013 A. M. Kolomeyer and D. S. Chu. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Purpose. To report the use of Descemet stripping endothelial keratoplasty (DSEK) in a patient with keratoglobus and chronic hydrops. Case Report. We describe a case of a 28-year-old man with bilateral keratoglobus and chronic hydrops in the right eye secondary to spontaneous Descemet membrane tear. The patient presented with finger counting (CF) vision, itching, foreign body sensation, and severe photophobia in the right eye. Peripheral corneal thinning with central corneal protrusion and Descemet mem- brane tear spanning from 4 to 7 o’clock was noted on slit lamp examination. The right eye cornea was 15 mm in the horizontal diam- eter. -
Corneal Ectasia
Corneal Ectasia Secretary for Quality of Care Anne L. Coleman, MD, PhD Academy Staff Nicholas P. Emptage, MAE Nancy Collins, RN, MPH Doris Mizuiri Jessica Ravetto Flora C. Lum, MD Medical Editor: Susan Garratt Design: Socorro Soberano Approved by: Board of Trustees September 21, 2013 Copyright © 2013 American Academy of Ophthalmology® All rights reserved AMERICAN ACADEMY OF OPHTHALMOLOGY and PREFERRED PRACTICE PATTERN are registered trademarks of the American Academy of Ophthalmology. All other trademarks are the property of their respective owners. This document should be cited as follows: American Academy of Ophthalmology Cornea/External Disease Panel. Preferred Practice Pattern® Guidelines. Corneal Ectasia. San Francisco, CA: American Academy of Ophthalmology; 2013. Available at: www.aao.org/ppp. Preferred Practice Pattern® guidelines are developed by the Academy’s H. Dunbar Hoskins Jr., MD Center for Quality Eye Care without any external financial support. Authors and reviewers of the guidelines are volunteers and do not receive any financial compensation for their contributions to the documents. The guidelines are externally reviewed by experts and stakeholders before publication. Corneal Ectasia PPP CORNEA/EXTERNAL DISEASE PREFERRED PRACTICE PATTERN DEVELOPMENT PROCESS AND PARTICIPANTS The Cornea/External Disease Preferred Practice Pattern® Panel members wrote the Corneal Ectasia Preferred Practice Pattern® guidelines (“PPP”). The PPP Panel members discussed and reviewed successive drafts of the document, meeting in person twice and conducting other review by e-mail discussion, to develop a consensus over the final version of the document. Cornea/External Disease Preferred Practice Pattern Panel 2012–2013 Robert S. Feder, MD, Co-chair Stephen D. McLeod, MD, Co-chair Esen K. -
Megalocornea Jeffrey Welder and Thomas a Oetting, MS, MD September 18, 2010
Megalocornea Jeffrey Welder and Thomas A Oetting, MS, MD September 18, 2010 Chief Complaint: Visual disturbance when changing positions. History of Present Illness: A 60-year-old man with a history of simple megalocornea presented to the Iowa City Veterans Administration Healthcare System eye clinic reporting visual disturbance while changing head position for several months. He noticed that his vision worsened with his head bent down. He previously had cataract surgery with an iris-sutured IOL due to the large size of his eye, which did not allow for placement of an anterior chamber intraocular lens (ACIOL) or scleral-fixated lens. Past Medical History: Megalocornea Medications: None Family History: No known history of megalocornea Social History: None contributory Ocular Exam: • Visual Acuity (with correction): • OD 20/100 (cause unknown) • OS 20/20 (with upright head position) • IOP: 18mmHg OD, 17mmHg OS • External Exam: normal OU • Pupils: No anisocoria and no relative afferent pupillary defect • Motility: Full OU. • Slit lamp exam: megalocornea (>13 mm in diameter) and with anterior mosaic dystrophy. Iris-sutured posterior chamber IOLs (PCIOLs), stable OD, but pseudophacodonesis OS with loose inferior suture evident. • Dilated funduscopic exam: Normal OU Clinical Course: The patient’s iris-sutured IOL had become loose (tilted and de-centered) in his large anterior chamber, despite several sutures that had been placed in the past, resulting now in visual disturbance with movement. FDA and IRB approval was obtained to place an Artisan iris-clip IOL (Ophtec®). He was taken to the OR where his existing IOL was removed using Duet forceps and scissors. The Artisan IOL was placed using enclavation iris forceps. -
Differences in Manifestations of Marfan Syndrome, Ehlers-Danlos Syndrome, and Loeys-Dietz Syndrome
1/30/2019 Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Ann Cardiothorac Surg. 2017 Nov; 6(6): 582–594. PMCID: PMC5721110 doi: 10.21037/acs.2017.11.03: 10.21037/acs.2017.11.03 PMID: 29270370 Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Josephina A. N. Meester,1 Aline Verstraeten,1 Dorien Schepers,1 Maaike Alaerts,1 Lut Van Laer,1 and Bart L. Loeys 1,2 1Center of Medical Genetics, Faculty of Medicine and Health Sciences, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium; 2Department of Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Corresponding author. Correspondence to: Bart L. Loeys. Center for Medical Genetics, University of Antwerp, Antwerp University Hospital, Prins Boudewijnlaan 43/6, 2650 Antwerp, Belgium. Email: [email protected]. Received 2017 Jul 1; Accepted 2017 Oct 9. Copyright 2017 Annals of Cardiothoracic Surgery. All rights reserved. Abstract Many different heritable connective tissue disorders (HCTD) have been described over the past decades. These syndromes often affect the connective tissue of various organ systems, including heart, blood vessels, skin, joints, bone, eyes, and lungs. The discovery of these HCTD was followed by the identification of mutations in a wide range of genes encoding structural proteins, modifying enzymes, or components of the TGFβ-signaling pathway. Three typical examples of HCTD are Marfan syndrome (MFS), Ehlers-Danlos syndrome (EDS), and Loeys-Dietz syndrome (LDS). These syndromes show some degree of phenotypical overlap of cardiovascular, skeletal, and cutaneous features. MFS is typically characterized by cardiovascular, ocular, and skeletal manifestations and is caused by heterozygous mutations in FBN1, coding for the extracellular matrix (ECM) protein fibrillin-1. -
Contact Lens Options and Fitting Strategies for the Management of the Irregular Cornea
6/23/2017 CONTACT LENS OPTIONS AND FITTING STRATEGIES FOR THE MANAGEMENT OF THE IRREGULAR CORNEA DAVID I. GEFFEN, OD, FAAO David I Geffen, OD, FAAO Consultant/Advisor/Speaker Accufocus Shire Alcon Tear Lab AMO Tear Science Annidis Bausch + Lomb TLC Vision Bruder Healthcare EyeBrain Optovue Revision Optics 1 6/23/2017 Irregular Cornea Contact Lens Options Standard Soft Lenses Custom Keratoconic Soft Lenses Corneal Gas Permeable Lenses Intra-Limbal Gas Permeable Lenses Piggyback and Recess Systems Scleral Gas Permeable Lenses Hybrid Lenses Types of Irregular Corneas DEGENERATIONS DYSTROPHIES • Keratoconus • Cogan’s dystrophy • Bowman’s dystrophy • Keratoglobus • Granular corneal dystrophy • Pellucid marginal degeneration • Lattice corneal dystrophy • Terrien’s marginal degeneration • Meesmann’s corneal dystrophy • Salzmann’s nodular degeneration CORNEAL SCARRING • Ehlers-Danlos syndrome • After infection AFTER SURGERY • After trauma • Cornea transplant (PK, PKP) • Radial keratotomy (RK) • Photorefractive keratectomy (PRK) • Phototherapeutic keratectomy (PTK) • Epikeratophakia • LASIK 2 6/23/2017 CL Options: Soft Lenses Advantages: . Comfort . Centration (draping) . Corneal Protection Limitations: . Vision (due to draping effect) . Dehydration . Hypoxia /microbial contamination CL Options: Custom Soft KC Lenses Hydrokone (Visionary Optics) NovaKone (Alden) Kerasoft (dist. By B&L) Soft K (Acculens & Advanced Vision, & SLIC Labs) Continental Kone (Continental) Keratoconus lens (Gelflex) Soflex (Marietta) -
Molecular Genetics of Corneal Dystrophy
Molecular Genetics of Corneal Dystrophy A THESIS SUBMITTED FOR THE M.D. TO THE UNIVERSITY OF LONDON MOHAMED EL-ASHRY, MB CHB FRCS (Ed) CLINICAL RESEARCH FELLOW DEPARTMENT OF MOLECULAR GENETICS INSTITUTE OF OPHTHALMOLOGY UNIVERSITY COLLEGE LONDON BATH STREET LONDON AND MOORFIELDS EYE HOSPITAL CITY ROAD LONDON 2001 ProQuest Number: 10013866 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest. ProQuest 10013866 Published by ProQuest LLC(2016). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code. Microform Edition © ProQuest LLC. ProQuest LLC 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106-1346 Abstract Abstract Comeal dystrophies are inherited disorders characterised by progressive accumulation of deposits in the cornea causing visual impairment. They occur in either an autosomal dominant or recessive form and are usually manifested in the first few decades of life. The present classification is solely based on the layer or layers of the cornea involved. This study aimed at better understanding of the underlying molecular basis of such disorders via linkage to specific chromosomal loci and then mutation screening of the disease genes by means of amplification of the genomic DNA using polymerase chain reaction and then sequencing and restriction enzyme digest analysis. -
Blue Sclera with and Without Corneal Fragility (Brittle Cornea Syndrome) in a Consanguineous Family Harboring ZNF469 Mutation (P
in situ where disc and retinal assessments are essential Ophthalmic examination revealed visual acuity of no and for preoperative evaluation if therapeutic IOL ex- light perception OU. Both eyes were phthisical, had blue change to transparent media is considered. sclera, and were soft to palpation. Moreover, the observed ability of occlusive IOLs to General assessment revealed a well-nourished alert boy transmit infrared light suggests the potential for devel- with normal vital signs and chestnut-colored hair. Height, opment of infrared light–based assessment tools such as weight, and head circumference were age appropriate. Skin Snellen charts for this patient group. was thin, velvety, and without abnormal elasticity. Subcu- taneous veins were easily appreciated. There were scat- Chetan K. Patel, BSc, FRCOphth tered small scars on all extremities and a large one at the Imran H. Yusuf, MBChB (Hons), MRes right elbow where a small surgical incision had been made. Victor Menezo, FRCOphth There was no joint hypermobility (Beighton score 2/9) or Author Affiliations: Oxford Eye Hospital, John Rad- scoliosis. Oral inspection revealed grossly normal denti- cliffe Hospital, Oxford, England. tion and a slightly arched palate. Extremity assessment re- Correspondence: Dr Patel, Oxford Eye Hospital, Ox- vealed bilateral valgus foot (talipes valgus) and hallux val- ford Radcliffe Hospitals National Health Service Trust, gus, which were confirmed by plain-film radiography. West Wing, John Radcliffe Hospital, Headley Way, Head- Skeletal plain-film radiography showed normal bone den- ington, Oxford OX3 9DY, England (ckpatel@btinternet sities without evidence for fractures. Complete blood cell .com). count and electrolyte levels were within normal limits. -
Femtosecond Laser-Assisted Tuck-In Penetrating Keratoplasty for Advanced Keratoglobus with Endothelial Damage
CASE REPORT Femtosecond Laser-Assisted Tuck-In Penetrating Keratoplasty for Advanced Keratoglobus With Endothelial Damage Jorge L. Alió del Barrio, MD, PhD,*† Olena Al-Shymali, MD,*‡ and Jorge L. Alió, MD, PhD, FEBOphth*† thinning, especially peripherally, in which the normal stromal Purpose: To describe the outcomes of femtosecond laser-assisted thickness is frequently reduced to less than one-fifth.1 KTG tuck-in penetrating keratoplasty as a single-step surgical procedure often presents at birth and results in the globular protrusion of for visual and anatomical rehabilitation of patients with severe the cornea, leading to severe loss of vision as a result of extreme keratoglobus (KTG) and endothelial damage. myopia, irregular astigmatism, and scarring.2 Severe complica- Methods: tions frequently appear as acute corneal hydrops and corneal Two eyes of a 7-year-old patient with bilateral severe 1–3 KTG and previous corneal hydrops were operated. Assisted by the perforations occurring spontaneously or after minimal trauma. KTG has been described in both congenital and femtosecond laser, both donor and recipient corneas were prepared. 2 An 8.5-mm full-thickness donor tissue with a peripheral partial- acquired forms. The former has been associated with blue thickness rim of 1.25 mm was sutured into an 8.5-mm recipient bed sclera syndrome, osteogenesis imperfecta, Leber congenital amaurosis, and connective tissue disorders, such as Ehlers– with a previously dissected intralamellar peripheral pocket up to the 2,4,5 limbus. The graft was secured with 16 interrupted 10-0 nylon sutures Danlos or Marfan syndrome. Acquired KTG has been and the peripheral donor rim tucked into the host stromal pocket. -
Editorial Page on Keratoconus
Acta Scientific Ophthalmology Volume 1 Issue 3 November 2018 Editorial Editorial Page on Keratoconus Gowhar Ahmad* Department of Ophthalmology, University of Jammu and Kashmir, India *Corresponding Author: Gowhar Ahmad, Department of ophthalmology, University of Jammu and Kashmir, India. Received: October 23, 2018; Published: October 25, 2018 keratoconus is a degenerative disease characterised by non- 13. Mar fans - 14. Mitral valves prolapse syndrome fraction so patient presents with frequent changes in refraction inflammatory corneal ectasia their is progressive changes in re 15. Achondroplasia condition is usually bilateral more common at puberty with male 16. Topic dermatitis preponderance condition has base and apex of cone base is re- 17. Aniridia ferred to plauciod cornea and apex is referred to nipple cornea keratoconus is a visual disturbing disease and not a visual threat- 18. Cong cataracts ening disease complicated cases of this disease entity present as 19. ROP keratoglobus glaucoma and hydrops typical characterises of kera- Recent modalities in the treatment of keratoconus are toconus are 1. Crossed corneal linkage 1. Foods and ruptures in de smets membrane of cornea 2. Hybrid contact lenses 2. Munson’s sign that is distortion of lower lid margin 3. Customised contact lens caused by bulged corea when patient looks in downward 4. Scleral contact lens phase 5. Scleral contact lens 3. Fleisher’s ring which is brownish ring of hemosiderin at 6. Pegy contact lens base of cone 7. Intrastromal corneal ring 4. Enlarged or visible corneal nerves 8. lamellar keratoplasty. 5. Vogt strea which are present in post stroma of cornea dis- appear on pressing the cornea Associated conditions with keratoconus are as follows Volume 1 Issue 3 November 2018 1. -
Asteroides to Trimethoprim-Sulphamethoxazole.' Cular Invasion Or Lipid Infiltration
928 Letters protrusion occurs above the area of thinning, Br J Ophthalmol: first published as 10.1136/bjo.80.10.928 on 1 October 1996. Downloaded from whereas in keratoconus the maximal protru- sion occurs in the thinned area. Also, the iron lines typical ofkeratoconus are absent here. In keratoglobus thinming and protrusion occur over the entire cornea rather than in one area as in this case. The unilateral presentation in this case is unusual, for PMD is considered a bilateral condition."2 Although bilateral conditions often present asymmetrically in degree or time, the left eye in this case shows no signs of corneal involvement 30 years after the first eye Figure 1 (A) Photograph of right eye showing became symptomatic and past the age that cornealprotrusion. (B) Slit-lamp photograph of PMD typically is diagnosed. Cases of unilat- same eye showing band ofclear corneal thinning Figure 1 Slit-lamp photograph, showing the 1-2 mm above limbus. eral PMD associated with other corneal thin- central corneal infiltrate (arrow). Two satellites ning disorders such as keratoconus in the can be discerned. The corresponding visual acuity opposite eye have been reported,34 but this is was 201200. the first case of isolated unilateral PMD in an elderly patient. BRET B WAGENHORST Columbia, SC 29209, USA Accepted for publication 24 May 1996 1 Krachmer JH. Pellucid marginal corneal degen- eration. Arch Ophthalmol 1978;%: 1217-21. 2 Krachmer JH, Feder RS, Belin MW. Kerato- conus and related noninflammatory corneal IW W;W' 'M- thinning disorders. Surv Ophthalmol 1984;28: 293-322. Figure 2 Light microscopy ofcorneal scraping 3 Lisch K. -
Keratoglobus After Long Standing Keratoconus - a Rare Case
Jemds.com Case Report Keratoglobus after Long Standing Keratoconus - A Rare Case Pravin K. Tidke1, Neha Bajpayee2 1, 2 Department of Ophthalmology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences (Deemed to Be University), Sawangi (Meghe), Wardha, Maharashtra, India. INTRODUCTION Keratoglobus can be congenital or acquired. Congenital form always is associated Corresponding Author: with connective tissue disorder like Ehlers Danlos syndrome type 4 and blue sclera Dr. Neha Bajpayee, S-16 Shalintai PG Girls Hostel, syndrome. Acquired form occurs in later stages of life and can be associated with Datta Meghe Institute of Medical keratoconjunctivitis, pellucid marginal degeneration, and is a severe form of Sciences (Deemed to Be University), keratoconus. Keratoglobus is a minimally progressive disorder and when presents Sawangi (Meghe), Wardha, with keratoconus, corneal thickness is compromised, thus, proper evaluation of Maharashtra, India. cornea is needed. Since prevalence of keratoglobus in Central India is 2.3 %, and E-mail: [email protected] association of this with keratoconus makes this case more unusual to study and report. DOI: 10.14260/jemds/2021/87 Keratoglobus is non-inflammatory and ectatic disorder of cornea which causes How to Cite This Article: corneal thinning from limbus to limbus and leads to globular protrusion of cornea.1 Tidke PK, Bajpayee N. Keratoglobus after In past keratoglobus was misdiagnosed as megalocornea or congenital glaucoma.2 long standing keratoconus- a rare case. J The -
Contact Lens Fitting: a Guide and Methodology of Contact Lens Fitting
Contact Lens Fitting: A Guide and Methodology of Contact Lens Fitting ISBN: 978-1-946628-15-2 01 Contact Lens Fitting: A Guide and Methodology of Contact Lens Fitting Aliki Kantzou* Saera University, Spain *Corresponding author Aliki Kantzou, Saera University, The School of Advanced Education, Research and Accreditation, Universidad Isabel I, Spain, Email: [email protected] Published By : Juniper publishers Inc. United States Date: June 23, 2018 Index 1. Abstract 2. Introduction 2.1. Theme 1. Contact Lenses Correct Refractive Errors a) Slit Lamp Examination b) Topography c) Contact Lens Fitting 2.2. Theme 2. Soft Spherical and Soft Toric Lenses A. Types of Soft Contact Lenses 2.3. Theme 3. Contact Lenses for Presbyopia a) Types of Presbyopia Contact Lenses for Far and Near Vision 2.4. Theme 4. Extended Wear Contact Lenses 2.5. Theme 5. Rigid Gas Permeable Contact Lenses 2.6. Theme 6. Scleral Contact Lenses 2.7. Theme 7. Hybrid Contact Lenses i. Hybrid Contact Lenses using New Technology 2.8. Theme 8. Cosmetic and Prosthetic Contact Lenses 2.9. Theme 9. Therapeutic Contact Lenses 2.10. Theme 10. Colored Contact Lenses 2.11. Theme 11. Contact Lens Fitting in Aphakic Patients 2.12. Theme 12. Contact Lens Fitting in Orthokeratology 2.13. Theme 13. Contact Lens Fitting in Children 2.14. Theme 14. Contact Lens Fitting in Patients with Corneal Ectasia a. Pellucid Marginal Degeneration b. Keratoglobus c. Keratoconus 2.15. Contact Lenses after Keratoplasty 2.16. Contact Lens Fitting after Refractive Laser Procedures 2.17. PROSE Contact Lenses 2.18. Contact Lenses and Scuba Diving 2.19.