1. Sturge Weber Syndrome,Dimitri Disease,Encephalofacial Angiomatosis,Encephalotrig Sturge Weber Syndrome,Dimitri Disease,encephalofacial angiomatosis,EncephalotrigeminalAngiomatosis,Leptomeningeal Angiomatosis,Meningeal Capillary Angiomatosis http://www.icomm.ca/geneinfo/sturge.htm

Sturge Weber Syndrome,Dimitri Disease,Encephalofacial Angiomatosis,Encephalotrigeminal Angiomatosis,Leptomeningeal Angiomatosis,Meningeal Capillary Angiomatosis,Sturge-Kalischer-Weber Syndrome,Sturge-Weber Phakomatosis,SWS,Sturge Weber Syndrome,Dimitri Disease Encephalofacial Angiomatosis,Encephalotrigeminal Angiomatosis,Leptomeningeal Angiomatosis,Meningeal Capillary Angiomatosis,Sturge-Kalischer-Weber Syndrome,Sturge-Weber Phakomatosis,SWS For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Sturge-Weber Syndrome also known as: Leptomeningeal Angiomatosis Dimitri Disease Encephalofacial Angiomatosis Encephalotrigeminal Angiomatosis Meningeal Capillary Angiomatosis Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis SWS (as defined by the National Organization for Rare Disorders Sturge-Weber Syndrome is composed of three major symptoms. Excessive blood vessel growths (leptomeningeal angiomas) are accompanied by accumulations of calcium inside the brain, and seizures.

2. Sturge-Weber Syndrome (www.whonamedit.com) angiomatosis encephalofacialis, cerebrocutaneous angiomatosis, encephalofacial angiomatosis, encephalofacial neuroangiomatosis, encephalotrigeminal syndrome, encephalotrigeminal angiomatosis http://www.whonamedit.com/synd.cfm/1764.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Sturge-Weber syndrome Also known as: Dimitri’s hemangiomatosis syndrome Jahnke's syndrome (variant without glaucoma) Kalischer's syndrome Krabbe's syndrome II Lawford's syndrome Lawford’s meningocutaneous syndrome Miller's syndrome Parkes Weber's syndrome Parkes Weber-Dimitri syndrome Schirmer's syndrome Sturge's syndrome Sturge-Kalischer-Weber syndrome Sturge-Parkes Weber-Dimitri syndrome Sturge-Weber-Krabbe syndrome Sturge-Weber-Thoma syndrome Weber's syndrome Weber-Dimitri syndrome Synonyms: Angioma capillare et venosum calcificans, angiomatosis encephalofacialis, cerebrocutaneous angiomatosis, congenital neuroectodermal dysplasia, cutaneocerebral angioma, cutaneodermal angioma, encephalocutaneous angiomatosis, encephalofacial angiomatosis, encephalofacial neuroangiomatosis, encephalotrigeminal syndrome, encephalotrigeminal angiomatosis, encephalotrigeminal vascular syndrome, facial-meningeal angiomas, fourth phacomatosis syndrome, meningeal capillary angiomatosis, meningofacial angiomatosis, meningo-oculofacial angiomatosis, neuroangiomatosis encephalofacialis, neurocutaneous syndrome, neuroectodermal hamartoma, neuro-oculocutaneous angiomatosis, neurooculocutaneous syndrome, naevoid amentia, trigemino-encephalo-angiomatosis, phacomatosis syndrome, vascular encephalotrigeminal syndrome.

3. Dorlands Medical Dictionary bacillary angiomatosis,   a condition seen in immunocompromised patients, caused by encephalofacial angiomatosis,   encephalotrigeminal angiomatosis,   SturgeWeber syndrome. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

4. EMedicine - Sturge-Weber Syndrome : Article Excerpt By: James J Riviello, Jr, MD SturgeWeber Syndrome - The Sturge-Weber syndrome (SWS), also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas involving the leptomeninges (leptomeningeal Related Terms encephalotrigeminal angiomatosis, encephalofacial angiomatosis, Sturge-Weber-Dimitri http://www.emedicine.com/neuro/byname/sturge-weber-syndrome.htm

(advertisement) Excerpt from Sturge-Weber Syndrome Synonyms, Key Words, and Related Terms: encephalotrigeminal angiomatosis, encephalofacial angiomatosis, Sturge-Weber-Dimitri syndrome Please click here to view the full topic text: Sturge-Weber Syndrome Background: The Sturge-Weber syndrome (SWS), also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas involving the leptomeninges (leptomeningeal angiomas [LAs]) and skin of the face, typically in the ophthalmic (V1) and maxillary (V2) distributions of the trigeminal nerve. The cutaneous angioma is called a port-wine stain (PWS). In the brain, LAs demonstrated by structural neuroimaging may be unilateral or bilateral; unilateral angiomas are more common. Functional neuroimaging may demonstrate a greater area of involvement than structural neuroimaging. This is called a structural versus functional mismatch. The neurologic manifestations vary, depending on the location of the LAs, which most commonly are located in the parietal and occipital regions, and the secondary effects of the angioma. These include seizures, which may be intractable; focal deficits, such as hemiparesis and hemianopia, both of which may be transient, called "strokelike episodes"; headaches; and developmental disorders, including developmental delay, learning disorders, and mental retardation. Developmental disorders are more common when angiomas are bilateral. Seizure control is thought to improve the neurologic outcome, and epilepsy surgery may be beneficial for refractory seizures.

5. EMedicine - Sturge-Weber Syndrome : Article Excerpt By: Ali Nawaz Khan, MBBS, FR angiomatosis, trigeminal angiomatosis, meningofacial angiomatosis, encephalofacial angiomatosis, Dimitris http://www.emedicine.com/radio/byname/sturge-weber-syndrome.htm

(advertisement) Excerpt from Sturge-Weber Syndrome Synonyms, Key Words, and Related Terms: SWS, Sturge-Weber-Dimitri syndrome, encephalotrigeminal angiomatosis, trigeminal angiomatosis, meningofacial angiomatosis, encephalofacial angiomatosis, Dimitri’s hemoangiomatosis, Jahnke’s syndrome (variant without glaucoma), Kulisher’s syndrome, Krabbe’s II syndrome, Lawford’s syndrome (variant with glaucoma and without increased ocular pressure), meningocutaneous syndrome, neurooculocutaneous syndrome, Parkes Weber’s phacomatosis, vascular encephalotrigeminal Weber-Dimitri syndrome Please click here to view the full topic text: Sturge-Weber Syndrome Background: Sturge-Weber syndrome (SWS) is a congenital disorder caused by the persistence of the transitory primordial sinusoidal plexus stage of vessel development. SWS is usually sporadic and characterized by a vascular malformation, with capillary venous angiomas that involve the face, choroid of the eye, and leptomeninges. The facial angioma has a predilection for the distribution of the first division of the trigeminal nerve. In addition to the angiomatous meningeal malformation, an underlying atrophy of the cerebral hemisphere is often present. The disease process is usually unilateral. Most patients (80%) have epilepsy, and more than 50% have a mental deficiency. Pathophysiology: Cranial manifestations The pathologic lesions in SWS include angiomatous facial malformation (port-wine stain or nevus flammeus), and venous angiomas involving the leptomeninges and choroid plexus. These lesions lead to seizures, atrophy, cerebrovascular thrombosis, and dystrophic intracortical calcification. Several variants of cortical calcification have been reported; these include calcification, which is present at birth (Yeakley, 1992); bilateral calcification (15%); and calcification contralateral to the facial nevus.

6. NORD - National Organization For Rare Disorders, Inc. encephalofacial angiomatosis. Encephalotrigeminal Angiomatosis. Leptomeningeal Angiomatosis. Meningeal Capillary Angiomatosis http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Sturge Weber

7. Syndrome DB - Table Of Contents angiomatosis. encephalofacial angiomatosis. encephalofacial neuroangiomatosis. encephalotrigeminal angiomatosis http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_e.html

Multiple Congenital Anomaly/Mental Retardation Syndromes Table of Contents Return to Entry Page A B C ... Z E Eagle-Barrett syndrome ear-patella-short stature (EPS) syndrome early onset parkinsonism-mental retardation syndrome early-onset diabetes mellitus-epiphyseal dysplasia syndrome ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 20 November 2001

8. Neuropsychology the leptomeningeal angiomatosis characteristic of encephalofacial angiomatosis (SturgeWeber Disease affected hemisphere. Angiomatosis ( Encephalofacial; Sturge-Weber Disease) This http://braincampus.learnpsychology.com/neupath/tumor/angiomat.html

Syllabus/Home Tumor Main Page Angiomatosis Astrocytoma ... Tumor Diagnosis and Treatment Angiomatosis This image depicts the leptomeningeal angiomatosis characteristic of encephalofacial angiomatosis (Sturge-Weber Disease). Note the mild atrophy of the affected hemisphere. Angiomatosis (Encephalofacial; Sturge-Weber Disease): This is a developmental disorder that involves a capillary-venous angioma of the face and leptomeninges of the brain. The facial angioma is also called a nevus flammeus or "port wine stain". Most lesions are unilateral. Although the angioma is present at birth, the neurological manifestations of the disorder emerge over the course of development. They may include focal seizures, contralateral spastic hemiplegia, hemisensory loss and visual field defects. There may be cortical atrophy and calcifications.

9. Sturge Weber Syndrome disorder subdivision(s) covered by this report. Synonyms Dimitri Disease;encephalofacial angiomatosis; Encephalotrigeminal Angiomatosis; http://my.webmd.com/hw/raising_a_family/nord306.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Sturge Weber Syndrome Important It is possible that the main title of the report Sturge Weber Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Dimitri Disease Encephalofacial Angiomatosis Encephalotrigeminal Angiomatosis Leptomeningeal Angiomatosis Meningeal Capillary Angiomatosis Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis SWS Disorder Subdivisions None General Discussion Sturge-Weber Syndrome is composed of three major symptoms. Excessive blood vessel growths (leptomeningeal angiomas) are accompanied by accumulations of calcium inside the brain, and seizures. Facial birth marks (nevus flammeus) appear usually on one side of the face. Angiomas similar to those found in the brain can develop inside the eye, often with secondary glaucoma. Resources The Arc (a national organization on mental retardation) 1010 Wayne Ave Suite 650 Silver Spring, MD 20910

10. Index Encephalitis, Japanese Encephalitis, Rasmussen s Encephalocele encephalocraniocutaneouslipomatosis encephalofacial angiomatosis Encephalopathy, Hypoglycemic http://my.webmd.com/hw/index/index-topics-E.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Support Organizations Search the Help Health Topics Click a letter to see a list of topics beginning with that letter A B C D ... EY E- E-D Syndrome back to top E. E. coli Infection back to top EA Eagle-Barrett Syndrome Eales Disease Eales Retinopathy Ear Anomalies-Contractures-Dysplasia of Bone with Kyphoscoliosis ... back to top EB EB EBV Susceptibility (EBVS) back to top EC ECD ECPSG Ectodermal and Mesodermal Dysplasia with Osseous Involvement Ectodermal and Mesodermal Dysplasia, Congenital ... back to top ED EDA Edema, Idiopathic EDMD EDS ... back to top EE EEC Syndrome back to top EF EFE Effective tooth brushing and flossing Effort Syndrome back to top EG EG back to top EH EHBA EHK Ehlers Danlos Syndrome back to top EI Eisenmenger Complex Eisenmenger Disease Eisenmenger Reaction Eisenmenger Syndrome ... back to top EK Ekman-Lobstein Disease Ektrodactyly of the Hand EKV back to top EL Elastorrhexis, Generalized

11. Definitions Of Genetic Disorders-E. htm Encephalitis Periaxialis Diffusa ald.htm Encephalitis Periaxialis Concentricabalo.htm Encephalocele encepha.htm encephalofacial angiomatosis sturge.htm http://www.icomm.ca/geneinfo/def-e.htm

For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Definitions of Genetic Disorders beginning with the letter E Click on the link next to the disorder to view its definition. E-D Syndrome eds.htm Eagle-Barrett Syndrome pbs1.htm Eales Retinopathy eales.htm Eales Disease eales.htm Ear Anomalies-Contractures-Dysplasia of Bone with Kyphoscoliosis beals.htm Ear Patella Short Stature Syndrome epsss.htm Early Constraint Defects amniot.htm Early Hypercalcemia Syndrome with Elfin Facie williams.htm Early-onset Dystonia dystonia.htm Eaton Lambert Syndrome lambert.htm EB epidbullo.htm Ebstein's anomaly congheart.html EBV Susceptibility (EBVS) xlp.htm EBVS xlp.htm ECD ecd.htm ECPSG epsich.htm Ectodermal Dysplasias ed.htm Ectodermal Dysplasia Anhidrotic with Cleft Lip and Cleft Palate rapphodkins.htm

12. Sturge Weber Syndrome this report. Synonyms. Dimitri Disease; encephalofacial angiomatosis;Encephalotrigeminal Angiomatosis; Leptomeningeal Angiomatosis; http://www.bchealthguide.org/kbase/nord/nord306.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord306"; var hwDocTitle="Sturge Weber Syndrome"; var hwRank="1"; var hwSectionHWID="nord306"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Sturge Weber Syndrome Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Dimitri Disease Encephalofacial Angiomatosis Encephalotrigeminal Angiomatosis Leptomeningeal Angiomatosis Meningeal Capillary Angiomatosis Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis SWS Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Neurofibromatosis (NF) Tuberous Sclerosis Von Hippel-Lindau Syndrome General Discussion Sturge-Weber Syndrome is composed of three major symptoms. Excessive blood vessel growths (leptomeningeal angiomas) are accompanied by accumulations of calcium inside the brain, and seizures. Facial birth marks (nevus flammeus) appear usually on one side of the face. Angiomas similar to those found in the brain can develop inside the eye, often with secondary glaucoma. Symptoms Nevus Flammeus is a discoloration on the face which is the red color of port wine. In Sturge-Weber Syndrome this "port wine stain" is noted at birth and generally occurs on the same side of the head as the excessive blood vessel growths (leptomeningeal angiomatoses) in the brain which are accompanied by accumulations of calcium (intracranial calcifications). The port wine stain primarily occurs along the distribution of the trigeminal nerve in the face, although in some cases it does not appear at all. Approximately thirty seven percent of patients have portwine stains on both sides of the face. Involvement of the extremities or trunk, in addition to the face, occurs in up to thirty-six percent of patients. Although the discoloration usually affects only one side of the face, a slight extension over the midface occurs in approximately fifty percent of cases. The port wine stain tends to deepen in color with age, and nodular elevations may also develop.

13. Entrez PubMed Click here to read encephalofacial angiomatosis sparing the occipital lobe andwithout facial nevus on the spectrum of SturgeWeber syndrome variants? http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

14. Entrez PubMed Abstract, encephalofacial angiomatosis sparing the occipital lobe and without facialnevus on the spectrum of SturgeWeber syndrome variants? J Child Neurol. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Link&db=PubMed&dbFrom=PubMed&f

15. Untitled encephalofacial angiomatosis (4) http//directory.google.co.nz/Top/Health/ Conditions_and_Diseases encephalofacial angiomatosis@ (4) http//search.aol.com/cat.adp?id=168 layer http://www.healthmednet.com/ECT-ENL.htm

ECT - ENL ECT (Emission Computed Tomography) [medical-test-topic] http://content.health.msn.com/content/healthwise/106/26476.htm Ecthyma http://health.yahoo.com/encyclopedia/a.html Ecthyma http://www.healthcentral.com/library/library.cfm ecthyma http://www.healthanswers.com/patco/videos_main.asp ECTHYMA GANGRENOSUM (10) http://dermatlas.med.jhmi.edu/derm/ Ectodermal and Mesodermal Dysplasia with Osseous Involvement http://my.webmd.com/content/healthwise/30/7398 Ectodermal and Mesodermal Dysplasia with Osseous Involvement [nord] http://content.health.msn.com/content/healthwise/106/26476.htm Ectodermal and Mesodermal Dysplasia, Congenital http://my.webmd.com/content/healthwise/30/7398 Ectodermal and Mesodermal Dysplasia, Congenital [nord] http://content.health.msn.com/content/healthwise/106/26476.htm Ectodermal Dysplasia http://directory.ansme.com/health/168.html Ectodermal Dysplasia http://health.excite.com/ Ectodermal dysplasia http://health.yahoo.com/encyclopedia/a.html Ectodermal Dysplasia http://www.familyvillage.wisc.edu/card_ef.htm

16. Brain Tumor Brain Tumor Angiomatosis. This image depicts the leptomeningeal angiomatosischaracteristic of encephalofacial angiomatosis (SturgeWeber Disease). http://nanonline.org/nandistance/mtbi/NeuroIll/tumor/angio.html

Course Home Page Course Syllabus Course Modules Case Studies Resources Neuroanatomy Atlas Neurological Disorders Infectious Disease Cerebral Vascular Disease ... Brain Tumor Angiomatosis Astrocytoma Craniopharyngioma Dermoid Cyst Ependymoma ... References Communication WWW Links e-mail Links Message Board NAN NAN Home Page NAN distanCE info@nanonline.org National Academy of Neuropsychology. Neurological Disorders Brain Tumor Angiomatosis This image depicts the leptomeningeal angiomatosis characteristic of encephalofacial angiomatosis (Sturge-Weber Disease). Note the mild atrophy of the affected hemisphere. Angiomatosis (Encephalofacial; Sturge-Weber Disease): This is a developmental disorder that involves a capillary-venous angioma of the face and leptomeninges of the brain. The facial angioma is also called a nevus flammeus or "port wine stain". Most lesions are unilateral. Although the angioma is present at birth, the neurological manifestations of the disorder emerge over the course of development. They may include focal seizures, contralateral spastic hemiplegia, hemisensory loss and visual field defects. There may be cortical atrophy and calcifications.

17. CNS Syndromes Associated With Vascular Malformations SturgeWeber syndrome (encephalotrigeminal or encephalofacial angiomatosis) Extensivecapillary-venous malformation results in unilateral cerebral cortical http://moon.ouhsc.edu/kfung/JTY1/NeuroHelp/ZNG0DD02.htm

CNS Syndromes Associated with Vascular Malformations NeuroLearn NeuroHelp Malformations Syndromes that involve the brain ... Syndromes that involve the spinal cord. S yndromes that involve the brain Head Sturge-Weber syndrome (encephalotrigeminal or encephalofacial angiomatosis): Extensive capillary-venous malformation results in unilateral cerebral cortical atrophy associated with angioma on the face which frequently include distribution of the ophthalmic branch of the trigerminal nerve. Angiomas in other tissue including the meninges, mucous membrane, and choroid can also occur. Heriditary mechanism unknown. Von Hippel-Lindau disease This is a combination of of retinal angiomatosis and angioma that is histologically identical to hemangioblastoma, multiple hemangioblastomas (most frequently in the cerebellum), pheochromocytoma, pancreatic cysts and islet cell tumor, renal cysts and bilateral, often multiple renal cell carcinoma of the kidney, and in males, bilateral papillary cystadenoma of the epidydimis, hepatic cyst, and endolymphatic sac tumor in the petrous bone [Kemperm a nn G ... and Neumann HP, 1998

18. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/E 5); Encephalitis@ (9); encephalofacial angiomatosis@ (4); Encephalomyelitis@(2); Enchondromatosis@ (3); Encopresis@ (5); EndStage Renal http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/E

Match: sort by: relevance date Free Services Subscribe by email RSS newsfeeds PDA-friendly format loc="/images/" A A A Find Jobs In: Healthcare Engineering Accounting College Contract / Freelance Customer Service Diversity Engineering Executive Healthcare Hospitality Human Resources Information Tech International Manufacturing Nonprofit Retail All Jobs by Job Type All Jobs by Industry Relocating? Visit: Moving Resources Moving Companies Mortgage Information Mortgage Calculator Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Conditions and Diseases E (0 links) Eagle-Barrett Syndrome Ear Infections - Children Eating Disorders Ebola ... Eye Cancer News about E [ More news about E Books about E Amazon.com's Price: Prices subject to change. Chemistry: The Central Science (Book with CD-ROM for Windows/MacIntosh by: Theodore L. Brown H. Eugene Lemay Jr. Bruce Edward Bursten Julia R. Burdge ... Theodore E. Brown May, 2002 List Price: Amazon.com's Price: You Save: Prices subject to change. The New 8-Week Cholesterol Cure : The Ultimate Program for Preventing Heart Disease by: Robert E. Kowalski

19. ÇáúÊöåÇÈõ ÇáÃóæÚöíóÉö ÇáÈóíÖÇÁ Translate this page encephalofacial angiomatosis, æõÑÇãñ æöÚóÇÆöíøñ ÏöãÇÛöíøñæóÌúåöíøñ ( ãõÊóáÇÒöãóÉõ ÓÊíÑÌ- æíÈÑ) º, http://www.emro.who.int/umd/BrowsingDic.asp?PageNo=11&Char=A

20. AKAs [Web Review Of Ophthalmology] @ WebEyeMD.com Retinal angiomatosis. SturgeWeber syndrome, encephalofacial angiomatosis. Spheroidaldegeneration, Climatic droplet keratopathy. Labrador’s keratopathy. http://webeyemd.com/wro/wro_aka.htm

Back to Home Web Review of Ophthalmology AKAs Age-Related Macular Degeneration (AMD) Age-related maculopathy Senile macular degeneration Dystrophy – any disorder arising from defective or faulty nutrition Granular corneal dystrophy – stroma clear? Groenouw’s type I Macular corneal dystrophy – indistinct irregular borders, intervening cloudy stroma Groenouw’s type II Lattice corneal dystrophy Biber-Haab-Dimmer dystrophy Epithelial dystrophy MDF dystrophy; map-dot-fingerprint dystrophy Cogan’s microcystic dystrophy ABMD; anterior basment membrane dystrophy Grave's Eye Disease Thyroid ophthalmopathy Thyroid orbitopathy Thyroid-related immune orbitopathy (TRIO) Von Basedow eye disease (in European literature) Large cell lymphoma Histiocytic lymphoma (old literature) Reticulum cell sarcoma (old literature) Phacoantigenic endophthalmitis

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 1     1-20 of 88    1  | 2  | 3  | 4  | 5  | Next 20