21. HONselect - Enchondromatosis enchondromatosis Enchondroma, Multiple - Enchondrosis, Multiple - Maffucci Syndrome - Ollier's Disease - Ollier Disease - Disease, Ollier http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

22. Ollier Disease Multiple enchondromatosis; Multiple Cartilaginous Enchondroses; Dyschondroplasia;enchondromatosis. Disorder Subdivisions. None. General Discussion http://my.webmd.com/hw/raising_a_family/nord337.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Ollier Disease Important It is possible that the main title of the report Ollier Disease 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 Multiple Enchondromatosis Multiple Cartilaginous Enchondroses Dyschondroplasia Enchondromatosis Disorder Subdivisions None General Discussion Ollier disease is a rare skeletal disorder characterized by abnormal bone development (skeletal dysplasia). While this disorder may be present at birth (congenital); it may not become apparent until early childhood when symptoms, such as deformities or improper limb growth, are more obvious. Ollier disease primarily affects the long bones and cartilage of the joints of the arms and legs, specifically the area where the shaft and head of a long bone meet (metaphyses). The pelvis is often involved; and even more rarely, the ribs, breast bone (sternum), and/or skull may also be affected. Ollier disease manifests as greater than normal growth of the cartilage in the long bones of the legs and arms so that growth is abnormal and the outer layer (cortical bone) of the bone becomes thin and more fragile. These masses of cartilage are benign (non-cancerous) tumors known as enchondromas. Enchondromas may occur at anytime. After puberty these growths stabilize as cartilage is replaced by bone. In rare cases, the enchondromas may undergo malignant changes (e.g., chondrosarcomas). The exact cause of Ollier disease is not known, although in some cases it may be inherited as an autosomal dominant genetic trait.

23. Maffucci Syndrome Dyschondrodysplasia with Hemangiomas; enchondromatosis with Multiple CavernousHemangiomas; Hemangiomatosis Chondrodystrophica; Kast Syndrome http://my.webmd.com/hw/raising_a_family/nord433.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Maffucci Syndrome Important It is possible that the main title of the report Maffucci 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 Dyschondrodysplasia with Hemangiomas Enchondromatosis with Multiple Cavernous Hemangiomas Hemangiomatosis Chondrodystrophica Kast Syndrome Multiple Angiomas and Endochondromas Disorder Subdivisions None General Discussion Maffucci Syndrome is a rare genetic disorder characterized by benign overgrowths of cartilage (enchondromas), skeletal deformities, and dark red irregularly shaped patches of skin (hemangiomas). Enchondromas are most often found in certain bones (phalanges) of the hands and feet. Skeletal malformations may include legs that are disproportionate in length and/or abnormal side-to-side curvature of the spine (scoliosis). In many cases, bones may tend to fracture easily. In most cases, hemangiomas appear at birth or during early childhood and may be progressive. Maffucci Syndrome is inherited as an autosomal dominant genetic trait. Resources American Cancer Society, Inc.

24. Enchondromatosis Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/ENCHONDROMATOS

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Enchondromatosis, presence of multiple foci of cartilage within bones and subperiosteal deposition of cartilage, involving one side of the body exclusively or predominantly. This disorder is nonhereditary and is also termed Ollier's disease. The tumours occur most frequently in the extremities but may also be found in the flat bones, such as those of the pelvis. Affected bones may be shortened and deformed. Children with enchondromatosis may be susceptible to pathologic fractures, and adults may be at risk of malignant transformation to chondrosarcoma Radiographically, the tumours may appear as linear or columnar radiolucent regions in the metaphyses or flat bones, which represent sites of persistent cartilaginous tissue ( Fig.1 ). Erosion and proliferation of the bone surface are sometimes observed. A nonhereditary enchondromatosis with soft tissue haemangiomas that may undergo malignant transformation is known as Maffuccis syndrome DR/RB The Encyclopaedia of Medical Imaging Volume III 1 Enchondromatosis, Fig. 1

25. Multiple Enchondromatosis Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/MULTIPLE ENCHOND

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Multiple enchondromatosis, see enchondromatosis multiple HC The Encyclopaedia of Medical Imaging Volume VII Corporate Products Financial Services Our Commitment ... Terms of Conditions

26. Radiology Case 438-3114 The lesions have well demarcated endosteal margins. Diagnosis, enchondromatosis,acroform, distal, expression. More information http://myweb.lsbu.ac.uk/dirt/museum/438-3114.html

no history available Diagnosis Analysis Analysis There are defects in the phalanges with some elevation of the edges, indicating expanding lesions in the bone. The lesions have well demarcated endosteal margins. Diagnosis: Enchondromatosis, acroform, distal, expression. ian@idmhome.demon.co.uk

27. Enchondromatosis - Enchondroma, Multiple - Information Page With HONselect Benign growths of cartilage in the metaphyses of several bones . http://www.hon.ch/HONselect/RareDiseases/EN/C05.116.099.708.338.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Enchondromatosis": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Enchondromatosis Definition: Benign growths of cartilage in the metaphyses of several bones. Synonym(s): Enchondroma, Multiple / Enchondrosis, Multiple / Maffucci Syndrome / Ollier's Disease / Browse New search Web resources for "Enchondromatosis" English French German Spanish = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - eMedicine - Maffucci Syndrome : Article by Raymond T Kuwahara, MD www.emedicine.com HONcode - NORD - National Organization for Rare Disorders, Inc. www.rarediseases.org II. Congenital and Hereditary Bone Disorders edcenter.med.cornell.edu HONcode - Virtual Children's Hospital: Paediapaedia: Enchondromatosis www.vh.org

28. HONselect - Enchondromatosis http://www.hon.ch/HONselect/RareDiseases/C05.116.099.708.338.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Enchondromatosis - Enchondroma, Multiple - Enchondrosis, Multiple - Maffucci Syndrome - Ollier's Disease - Ollier Disease - Disease, Ollier Français: Enchondromatose - Chondromatose multiple - Ollier, maladie - Maladie d'Ollier - Syndrome de Maffucci - Angiochondromatose de Maffucci Deutsch: Enchondromatose - Enchondromatose, multiple - Enchondrosis, multiple - Ollier-Krankheit - Maffucci-Syndrom Español: Encondromatosis - Encondroma Múltiple - Encondrosis Múltiple - Enfermedad de Ollier - Síndrome de Maffucci Português: Encondrose Múltipla - Doença de Ollier - Encondroma Múltiplo - Síndrome de Maffucci HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: No Web sites: English Yes Français Yes Deutsch Yes Español Yes Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C05.116.099.708.338.html Last modified: Wed May 18 2005

29. Enchondromatosis enchondromatosis Medical.WebEnds.com. enchondromatosis. Enchondroma, Multiple;Enchondrosis, Multiple; Maffucci Syndrome; Ollier s Disease; http://medical.webends.com/kw/Enchondromatosis

Medical.WebEnds.com - Medical Terminology Dictionary A B C D ... Z WWW Medical.WebEnds.com Enchondromatosis Benign growths of cartilage in the metaphyses of several bones. Google links Processing time was 0.024333000183105 seconds.

30. Multiple Enchodromatosis (Ollier's Disease) - Wheeless' Textbook Of Orthopaedics in some cases enchondromatosis will affect patients in the metaphyseal and epiphyseal Epiphyseal Metaphyseal enchondromatosis. A new clnical entity. http://www.wheelessonline.com/ortho/multiple_enchodromatosis_olliers_disease

Duke Orthopaedics presents Wheeless' Textbook of Orthopaedics Site Index A - Z Search Site by Word Home Contact Us My Account 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 and feet as well as long bones of upper and lower extremities; - limb length inequality may be of sufficient severity to require surgery; - 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;

31. The Malignant Potential Of Enchondromatosis - Wheeless' Textbook Of Orthopaedics The malignant potential of enchondromatosis of the brain and abdomen foroccult malignant lesions is indicated in patients who have enchondromatosis. http://www.wheelessonline.com/ortho/the_malignant_potential_of_enchondromatosis

Duke Orthopaedics presents Wheeless' Textbook of Orthopaedics Site Index A - Z Search Site by Word Home Contact Us My Account The malignant potential of enchondromatosis Steve Rowlands website graphic design at www.steverowlands.com http://www.DiamondSea.com

32. A Mutant PTH/PTHrP Type I Receptor In Enchondromatosis - Nature Genetics The extent of skeletal involvement is variable in enchondromatosis and may enchondromatosis is rare, obvious inheritance of the condition is unusual and http://www.nature.com/doifinder/10.1038/ng844

@import "/ng/style.css"; NATURE.COM NEWS@NATURE.COM NATUREJOBS NATUREEVENTS ... Help E-MAIL: PASSWORD: Save password Forgotten password? SEARCH JOURNAL Advanced search Journal home Archive Table of Contents ... For librarians NPG Resources Nature Nature Cell Biology Nature Medicine Nature Reviews Genetics ... Browse all publications Letter Nature Genetics A mutant PTH/PTHrP type I receptor in enchondromatosis Sevan Hopyan , Nalan Gokgoz , Raymond Poon , Robert C. Gensure , Chunying Yu , William G. Cole , Robert S. Bell , Irene L. Andrulis , Jay S. Wunder Program in Developmental Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada. Program in Molecular Biology and Cancer, Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G1X5, Canada. Department of Surgery, Division of Orthopaedics, University of Toronto, Toronto, Ontario, Canada. Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada. Endocrine and Pediatric Endocrine Units, Departments of Medicine and Pediatrics, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA. Division of Orthopaedics, The Hospital for Sick Children, Toronto, Ontario, Canada.

33. Enchondromatosis enchondromatosis. enchondromatosis. Dyschondroplasia. enchondromatosis, multiple.Maffucci syndrome. Ollier disease. Osteochondromatosis http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?cat3=106

34. Ollier Disease Synonyms. Multiple enchondromatosis; Multiple Cartilaginous Enchondroses;Dyschondroplasia; enchondromatosis. Disorder Subdivisions. None http://www.bchealthguide.org/kbase/nord/nord337.htm

var hwPrint=1;var hwDocHWID="nord337";var hwDocTitle="Ollier Disease";var hwRank="1";var hwSectionHWID="nord337-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Ollier Disease Important It is possible that the main title of the report Ollier Disease 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 Multiple Enchondromatosis Multiple Cartilaginous Enchondroses Dyschondroplasia Enchondromatosis Disorder Subdivisions None General Discussion Ollier disease is a rare skeletal disorder characterized by abnormal bone development (skeletal dysplasia). While this disorder may be present at birth (congenital); it may not become apparent until early childhood when symptoms, such as deformities or improper limb growth, are more obvious. Ollier disease primarily affects the long bones and cartilage of the joints of the arms and legs, specifically the area where the shaft and head of a long bone meet (metaphyses). The pelvis is often involved; and even more rarely, the ribs, breast bone (sternum), and/or skull may also be affected. Ollier disease manifests as greater than normal growth of the cartilage in the long bones of the legs and arms so that growth is abnormal and the outer layer (cortical bone) of the bone becomes thin and more fragile. These masses of cartilage are benign (non-cancerous) tumors known as enchondromas. Enchondromas may occur at anytime. After puberty these growths stabilize as cartilage is replaced by bone. In rare cases, the enchondromas may undergo malignant changes (e.g., chondrosarcomas). The exact cause of Ollier disease is not known, although in some cases it may be inherited as an autosomal dominant genetic trait.

35. Enchondromatosis - Talk Medical Humanfriendly medical definition of enchondromatosis. http://www.talkmedical.com/medical-dictionary/4846/Enchondromatosis

Home Medications Medical Dictionary Talk Medical ... Medical Dictionary Newsletter Subscribe to the free monthly health digest. Relevant health articles just for you. Tell a friend Enchondromatosis Enchondromatosis: A condition characterized by multiple enchondromas benign masses of cartilage growing within bones. The enchondromas can deform and shorten a limb and predispose to a fracture. The condition can be caused by a mutation in the gene for the parathyroid hormone receptor (PTHR1). Also known as Ollier disease. Print this page About Talk Medical Help Contact Us ... Terms and Conditions

36. Dorlands Medical Dictionary multiple congenital enchondromas, enchondromatosis. multiple enchondromatosis,skeletal enchondromatosis, enchondromatosis. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

37. Enchondromatosis Topic - Unified Search Environment enchondromatosis Topic Tree enchondromatosis MSH/MH/D004687 MTHICD9/ET/756.4 MSH/PM/D004687 Enchondroma, Multiple MSH/EP/D004687 MSH/PM/D004687 http://www.use.hcn.com.au/portals/shared/subject.`Enchondromatosis`/home.html

Enchondromatosis Topic Tree Definition: Benign growths of cartilage in the metaphyses of several bones. Synonyms and Source Vocabularies: Enchondromatosis Enchondroma, Multiple Enchondrosis, Multiple Ollier's Disease ENCHONDROSES, MULTIPLE, CARTILAGINOUS CHONDROMATOSIS, UNILATERAL ENCHONDROMATOSIS, MULTIPLE Bone Diseases, Developmental Basal Cell Nevus Syndrome Dwarfism Dysostoses ... Marfan Syndrome Osteochondrodysplasias Achondroplasia Chondrodysplasia Punctata Cleidocranial Dysplasia Diaphyseal Dysplasia, Progressive ... Acro-Osteolysis

38. Epiphyseal-Metaphyseal Enchondromatosis. A New Clinical Entity -- GABOS And BOWE EpiphysealMetaphyseal enchondromatosis. A New Clinical Entity*. PETER G. GABOS,MD {dagger} and J. RICHARD BOWEN, MD {dagger} , WILMINGTON, DELAWARE http://www.ejbjs.org/cgi/content/abstract/80/6/782

JBJS CME HELP FEEDBACK ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Full Text Full Text (PDF) Letters to the Editor: Submit a response ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Reprints and Permissions PubMed PubMed Citation Articles by GABOS, P. G. Articles by BOWEN, J. R. Related Collections Pediatric Disease Pediatrics Oncology Leg ... Pathology The Journal of Bone and Joint Surgery The Journal of Bone and Joint Surgery, Inc. Epiphyseal-Metaphyseal Enchondromatosis. A New Clinical Entity* PETER G. GABOS, M.D. and J. RICHARD BOWEN, M.D. , WILMINGTON, DELAWARE Investigation performed at the Alfred I. duPont Hospital for Children, Wilmington We reviewed the cases of eight unrelated children who had an unusual form of enchondromatosis characterized by unilateral enchondromas arising within the epiphyseal and metaphyseal regions of the long tubular bones of the lower extremity. Unlike previously

39. Entrez PubMed enchondromatosis/epidemiology* enchondromatosis/pathology enchondromatosis/surgeryFemale Granulosa Cell Tumor/epidemiology* Granulosa Cell Tumor/pathology http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9

40. Entrez PubMed enchondromatosis (Ollier disease, Maffucci syndrome) is a rare developmentaldisorder characterized by multiple enchondromas. Not much is known about its http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

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