61. Xray2000 Dyschondroplasia (enchondromatosis)(ollier s disease). Definition A rarely familial, proliferation of cartilage in the metaphyses http://www.xray2000.f9.co.uk/radpath/d/dyschondroplasia.htm

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62. Ollier's Disease (www.whonamedit.com) If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here see a doctor. ollier s disease http://www.whonamedit.com/synd.cfm/1813.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. Ollier's disease Synonyms: Chondrodysplasia, dyschondroplasia, enchondromatosis, hemichondrodysplasia, hemichondrodystrophy, internal chondromatosis, multiple enchondromata, multiple enchondromatosis, multiple enchondromata syndrome, osteochondromatosis syndrome. Associated persons: Angelo Maffucci Louis Xavier Édouard Léopold Ollier Description: A disorder of the growing ends of bones in which round nonossified cartilaginous masses scattered throughout the skeleton produce asymmetrical and very variable deformities, asymmetric leg shortening being common. The lesions are first noted from 1 to 4 years of age, rarely at birth, with little progression after adolescence. Both sexes may be affected. The majority of cases have been sporadic but a familial tendency has been reported in a few instances. Enchondromatosis is usually bilateral. The term Ollier syndrome applies in cases with unilateral involvement. The combination of multiple enchondromata with haemangiomata and phleboliths is known as Maffucci syndrome.

63. Louis Xavier Édouard Léopold Ollier (www.whonamedit.com) Associated with KlippelTrénaunay-Weber syndrome,ollier s disease,ollier s layer,ollier-Thiersch graft. Who named it? Home. List categories. ollier’s disease. http://www.whonamedit.com/doctor.cfm/477.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. Louis Xavier Édouard Léopold Ollier French surgeon, born December 2, 1830, Vans, département Ardèche; died November 26, 1900, Lyon. Associated eponyms: Klippel-Trénaunay-Weber syndrome A rare syndrome characterized by unilateral congenital capillary and cavernous haemangiomatous malformations of the arteriovenous system, syndactyly, overgrowth of certain fingers, and osteohypertrophic changes of one extremity. Ollier's disease A disorder of the growing ends of bones. Ollier's layer The inner layer of the periosteum, closest to the bone. Ollier-Thiersch graft A split-thickness skin graft. Biography: Louis Xavier Édouard Léopold Ollier is particularly remembered for his work on bone and joint surgery. He was born in Vans, Ardèche, where both his father and his grandfather had been doctors. He initially studied natural science at Montpellier and in 1849 was assistant in botany in the faculty of medicine.

64. Ollier's Disease ollier s disease. by Christina Gentle ArticleInsider.com % If brender = 0 Then % Check Out Our Suggested Site for ollier s disease Information! % End If % . http://www.deformitydepot.com/olliers-disease.html

@import "style.css"; Wednesday, June 2nd, 2004 Bookmark This Page Email This Page Limb Lengthening Arthritis ... Site Map Ollier's Disease by Christina Gentle ArticleInsider.com Ollier's disease is a defect which can be present from birth, but is not hereditary, that causes tumors to grow in the bones usually on one side of the body. Generally the long bones are affected like the femur or tibia, for example, and can also affect bones in the feet and hands. Tumor growth in the bones, caused by this disease can affect the growth plates, and if this occurs in one of the legs it can lead to a leg length discrepancy. Check Out Our Suggested Site for Ollier's Disease Information! An example case can be a child who shows signs of this disease by walking with a limp, and when observed more closely it may be noticed that one leg is shorter than the other. This occurrence can be a result of unossification, caused by Ollier's, which is when bone stops forming normally. In this particular form limb lengthening procedures can be performed to help lengthen the shorter leg to a close proximity of the longer one. Factors of Ollier's Disease The lumping and swelling which can occur around infected areas of bone can lead to outward lesions and can become infected if not cared for properly. Tumors around the bones in children with this disease are most likely benign, but in adults with other conditions the tumors can lead to malignant transformations. Deformities other than leg length discrepancy can appear, and when bones become very weak in children, fractures can become common.

65. Ollier's Disease Other characters, ollier s disease,. Print this article, (Louis ollier, 1830–1900, French orthopaedic surgeon), enchondromatosis multiple. http://www.amershamhealth.com/medcyclopaedia/Volume VII/OLLIERS DISEASE.asp

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Ollier's disease, (Louis Ollier, 1830–1900, French orthopaedic surgeon), enchondromatosis multiple GL The Encyclopaedia of Medical Imaging Volume VII Contacts GE Healthcare Making Waves

66. Ollier's Disease N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, ollier s disease,. Print this article, (Louis ollier, 18301900, French orthopaedic surgeon), enchondromatosis multiple. http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/OLLIERS DISEASE.

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Ollier's disease, (Louis Ollier, 18301900, French orthopaedic surgeon), enchondromatosis multiple GL The Encyclopaedia of Medical Imaging Volume VII Contacts GE Healthcare Making Waves

67. Ollier's Disease (Dyschondroplasia, [Multiple] Enchodromatosis, Osteochondromato HOME. ollier s disease (Dyschondroplasia, Multiple Hereditary Enchodromatosis, Osteochondromatosis). Simultaneous occurrence of http://www.bdid.com/ollier.htm

HOME Ollier's Disease (Dyschondroplasia, [Multiple] Hereditary Enchodromatosis, Osteochondromatosis) Simultaneous occurrence of a supra- and an infratentorial glioma in a patient with Ollier's disease: more evidence for non-mesodermal tumor predisposition in multiple enchondromatosis Atypical chondrodysplasia: a further variant of multiple enchondromatosis with vertebral involvement? Diffuse brain stem tumor in an adolescent with multiple enchondromatosis (Ollier's disease) Multiple Hereditary Exostoses ... Enchondroma (Includes X-Rays) Ollier's Disease Enchondromatosis HOME

68. Birth Disorder Information Directory - O Lethal Type See Young McKeever Squier Syndrome. ollier s disease (Dyschondroplasia, Multiple Enchodromatosis, Osteochondromatosis) http://www.bdid.com/defecto.htm

HOME O O'Doherty Syndrome (Cutaneous Albinism Hermine Phenotype, Ermine Phenotype, Pigmentary Disorder with Hearing Loss) Cutaneous albinism hermine phenotype ERMINE PHENOTYPE Also see Black Locks with Albinism and Deafness (BADS) Syndrome Obrinsky Syndrome See Prune Belly Syndrome Obstructive Uropathy See Posterior Urethral Valves Occipital Horn Syndrome (Ehlers Danlos Syndrome, Type IX) Information OCCIPITAL HORN SYNDROME Also see Cutis Laxa Ochoa Syndrome See Urofacial syndrome Ochronosis See Alkaptonuria(, Hereditary) Ochronotic Arthritis See Alkaptonuria(, Hereditary) Ocular Albinism See Albinism, Ocular Forsius Eriksson Type See Albinism, Ocular, Type II Oculo-Bucco-Genital Syndrome See Behcet Disease/Syndrome Oculoauriculovertebral (OAV) Dysplasia/Spectrum See Goldenhar (Gorlin) Syndrome Oculocerebral Hypopigmentation Syndrome Cross Type See Cross Syndrome Oculocerebrorenal (OCR) Syndrome chromosome 11p deletion syndrome Oculocutaneous Albinism (Albinism Oculocutaneous, Hermansky Pudlak Type; Albinism, Yellow Mutant Type; Delta-Storage Pool Disease; Hermansky Pudlak Syndrome; Kotzot Richter Syndrome) List of Sites Oculodento(digital/osseous) Dysplasia OCULODENTODIGITAL DYSPLASIA; ODDD

69. Ollier's Disease - General Practice Notebook ollier s disease. This is a familial cause of multiple, unilateral chondromata. Click here for more information The information http://www.gpnotebook.co.uk/cache/-1449525246.htm

Ollier's disease This is a familial cause of multiple, unilateral chondromata. Click here for more information...

70. Ollier's Disease - General Practice Notebook ollier s disease. Medical search. This is a familial cause of multiple, unilateral chondromata. http://www.gpnotebook.co.uk/medwebpage.cfm?ID=-1449525246

71. AAMED: American Association Of Multiple Enchondroma Diseases and registered as a tax exempt organization with the US Internal Revenue Service, AAMED is comprised of individuals with ollier s disease, Maffucci s syndrome http://www.aamed.net/

Navigation Home Downloads Encyclopedia FAQ ... Web Links Who's Online There are currently, 2 guest(s) and member(s) that are online. You are Anonymous user. You can register for free by clicking here The American Association of Multiple Enchondroma Diseases Welcomes You to Our Site! Founded in 1998, incorporated in 2002 as a not-for-profit corporation and registered as a tax exempt organization with the US Internal Revenue Service, AAMED is comprised of individuals with Ollier's disease, Maffucci's syndrome, enchondromatosis, their families, and physicians. AAMED is THE source for news and information about bone tumor diseases, research and services for adults and children with Enchondromatosis, Multiple Enchondroma, Ollier's disease, Maffucci's syndrome, and their families. On this site, you'll find links to our quarterly newsletters, message board, pen-pal program for children, latest research information, and much more. We invite interested persons to become part of group. Click on the membership link for more information on joining us. OUR ACTIVITIES participation in research projects to find treatments and a cure for these diseases helping families cope with the physical/psychological burdens imposed by the disease we provide a forum for patients and families to express their concerns and experiences connect individuals with common symptoms and backgrounds we continuously update a data base of physicians and hospitals with Ollier/Maffucci expertise Videos on limb lengthening and the use of the Ilizarov fixator

72. AAMED: American Association Of Multiple Enchondroma Diseases - Ollier's & Maffuc will update everyone on the latest information regarding both the clinical aspects as well as the current research findings of ollier s disease and Maffucci s http://www.aamed.net/modules.php?name=News&file=article&sid=3

73. Ollier's Disease : On Medical Dictionary Online ollier s disease defined on the Free Online Medical Dictionary. ollier s disease. Benign growths of cartilage in the metaphyses of several bones. http://www.online-medical-dictionary.org/?q=Ollier's Disease

74. Wheeless' Textbook Of Orthopaedics Main Menu Home Page Multiple Enchodromatosis (ollier s disease). Discussion The malignant potential of enchondromatosis ollier s disease. An http://www.wheelessonline.com/o6/93.htm

Main Menu Home Page Multiple Enchodromatosis (Ollier's Disease) - Discussion: - originally was described by Ollier in late 1800's; - characterized by multiple enchondroma lesions primarily located w/ in the metaphyseal regions of tubular bones; - usually diagnosed in childhood; - pts w/ Ollier's dz have increased risk of a secondary chondrosarcoma developing later in life; - risk is about 25% by age 40 yrs; - Clinical Findings: - most pts have bilateral involvement, w/ predominance on one side; - enchondromas most frequently involve the short tubular bones of hands - Radiographs: - in most cases, there will be diaphyseal lesions or metaphyseal lesions which do not cross the growth plate, at least, not until growth plate closure; - in some cases enchondromatosis will affect patients in the metaphyseal and epiphyseal regions; - when enchondromas cross the growth plate, severe limb length deformities and angular deformities will develop; The malignant potential of enchondromatosis Ollier's Disease. An assessment of angular deformity, shortening, and

75. Entrez PubMed Click here to read Malignant progression in multiple enchondromatosis (ollier s disease) an autopsybased molecular genetic study. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

76. Uhrad.com Pediatric Imaging Teaching Files Discussion Enchondromatosis (ollier s disease) is a non hereditary disorder of enchondral ossification with lesions distributed throughout the tubular and http://www.uhrad.com/pedsarc/peds055.htm

uhrad.com - Pediatric Imaging Teaching Files Case Fifty Five - Multiple Enchondromatosis Click on Images for Enlarged View Clinical History: Trauma to second right digit. Findings: Multiple lucent metaphyseal lesions of the proximal and middle phalanges of the fourth and fifth digits, as well as the distal metacarpals of the fourth and fifth digits. Diagnosis: Multiple enchondromatosis. Discussion: Enchondromatosis (Ollier's Disease) is a non hereditary disorder of enchondral ossification with lesions distributed throughout the tubular and flat bones of the body. The presenting clinical manifestations are masses that increase in size as the child grows, asymmetric limb shortening and either genu varus or genu valgus deformities. Radiographs of the young child could be normal in the first few years of life and later demonstrate radiolucent streaking within the metaphysis of involved bones, or at infancy may demonstrate radiolucent masses which can be round, triangular or linear. Stippled calcifications occur with age within the enchondromas. There may be considerable expansion of the tubular bones especially in the hands, and pathologic fractures may occur. Cartilaginous areas extending from the physis can lead to a growth interference resulting in limb shortening and deformities. Enchondromas typically stabilize or regress in adulthood. However, sarcomatous transformation has been described. Six types of enchondromatosis have been described, of which three are more common. If the multiple enchondromas are purely unilateral or unevenly distributed throughout the metaphyses of the long bones, sparing the cranium and spine, it is called Ollier's Disease. If the enchondromas are seen with multiple cutaneous hemangiomas (soft tissue calcifications/phleboliths) it is called Maffucci's Syndrome. If there is symmetric involvement throughout the body including the cranium, hands and feet, it is known as generalized enchondromatosis. The Ollier's and Maffucci's are more common in boys (2:1). The less frequent types include metachondromatosis which affects the short tubular bones of the hands and feet, and spondyloenchondroplasia in which the enchondromas are associated with platyspondyly, and enchondromas with irregular vertebral bodies.

77. Musculoskeletal Diseases Enchondromatosis. About ollier s disease xray2000.co.uk. ollier/Maffucci Self Help Group - (US). ollier s disease Self Help Group, UK. Fibrous Dysplasia of Bone. http://www.mic.ki.se/Diseases/C05.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Musculoskeletal Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Achondroplasia Achondroplasia Acquired Hyperostosis Syndrome Acrocephalosyndactylia ... Tietze's Syndrome Musculoskeletal Diseases Textbook of Orthopaedics [CR Wheeless] Educational textbook syllabus [Borrill et al.] - Orthoteers (UK) The Belgian OrthoWeb - (BE) Site Map of the Orthopaedics and Sports Medicine resource at Univ of Washington, Seattle (US) The American Academy of Orthopaedic Surgeons A Musculoskeletal Atlas and a set of educational cases (radiol.) - U of Washington (US) OrthoLinx WorldOrtho including A Simple Guide to Orthopaedics [RL Huckstep] - Nepean Hosp., Sydney (AU) A collection of Case discussions at OrthoGate.org An orthopedic Encyclopedia - for patients - DynoMed.com

78. Case Of The Month - January, 2003 Image 1 minimal disease. Image 2 19 year old. Image 3 19 tear old patient. Diagnosis Multiple Enchodromatosis (ollier s disease). Discussion http://cases.pedrad.org/case.php?month=January&year=2003

79. OLLIER'S DISEASE Definition Home/O/OL/ollier S disease. Medical Dictionary Search Engine. Advertise on this site! A service of healthlink-net.com. Browse Dictionary Alphabetically. http://www.books.md/O/dic/Olliersdisease.php

Home O OL /OLLIER'S DISEASE Medical Dictionary Search Engine Advertise on this site! A service of health-link-net.com Browse Dictionary Alphabetically A B C D ... Z Benign growths of cartilage in the metaphyses of several bones. Toys and Blankets Miami Rooms New York Hotels Travel Discounts ... Home

80. Endochondromatosis, Ollier's Disease, Dyschondroplasia Past Issue Volume 16, Number 4 • October 2003, Return to Table of Contents. PDF of this Article. Incidental skeletal abnormalities in a 22year-old man. http://www.baylorhealth.edu/proceedings/16_4/16_4_bufkin.htm

About Current Issue Past Issues Staff and Editorial Board ... Submit a Manuscript Site Search Past Issue: Return to Table of Contents PDF of this Article Incidental skeletal abnormalities in a 22-year-old man William J. Bufkin, MD A 22-year-old man presented to the emergency department because of trauma. Radiographic images are shown below. For diagnosis and discussion, see the following page. Directions and Map Contact Us Career Opportunities BaylorHealth.com ... Baylor Portal Login

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