Download Citation on ResearchGate | Encondromatosis múltiple, enfermedad de Ollier | Multiple enchondromatosis (Ollier’s disease) is a rare disease. Request PDF on ResearchGate | Enfermedad de Ollier: tumores benignos con riesgo de malignización. Revisión de 17 casos | AimTo review. Ollier disease is a skeletal disorder characterized by multiple enchondromas, which are noncancerous (benign) growths of cartilage that develop within the.
|Published (Last):||12 September 2007|
|PDF File Size:||1.92 Mb|
|ePub File Size:||1.12 Mb|
|Price:||Free* [*Free Regsitration Required]|
The documents contained in this web site are presented for information purposes only. Prevalence is estimated at around 1 inCiteScore measures average citations received per document published. Se continuar a navegar, consideramos que aceita o ollier uso. Synonyms or Alternate Spellings: Persons with Ollier disease are prone to breaking bones and normally have swollen, aching limbs.
Enchondromatosis | Radiology Reference Article |
Ollier disease is a rare nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors enchondroma develop close to growth plate cartilage. Maffucci syndrome carries a higher risk for cancer. D ICD – Case 1 Case 1. Subscribe to our Newsletter.
The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Log in Sign up. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
Professionals Summary information Greekpdf Review article English Disease definition Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones. Check for errors and try again. Edit article Share article View revision history. Ollier disease is not normally diagnosed until toddler years because it is not very visible.
Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s enfermedda Ollier disease.
Loading Stack – 0 images remaining. Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia. Check this box if you wish to receive a copy of your message. CiteScore measures average citations received per document published.
This section is empty. With age, the cartilage may calcify in the typical “snowflake” pattern. Show all Show less. In distinction from solitary lesions, enchondromas of enchondromatosis are more likely to be hypercellular enfermedaf nature, yet are still considered benign in the absence of other aggressive findings This page was last edited on 14 Octoberat More interestingly, it has been reported engermedad the PTHrP parathyroid hormone-related protein enfrrmedad has been implicated as a gene responsible for cases of enchondromatosis in patients with a family history of mild skeletal dysplasia in their male parents.
SRJ is a prestige metric based on the idea that not all citations are the same. Ollier disease is seen in both sexes without gender predilection and usually becomes apparent by early childhood 3,4. Previous article Next article.
Unable to process the form. You can change the settings or obtain more information by clicking here. You can enrermedad the settings or obtain more information by clicking here. For all other comments, please send your remarks via contact us.
Health care resources for this disease Expert centres Diagnostic tests 14 Patient organisations 50 Orphan drug s 0. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: These manuscripts contain updated topics with a major enfermedae or conceptual relevance in modern medicine. Are you a health professional able to prescribe or dispense drugs? Continuing navigation will be considered as acceptance of this use.
Once the individual stops growing then in general, so do the enchondromas. Detailed information Article for general public Svenska Are you a health professional able to prescribe or dispense drugs?
Orphanet: Enfermedad de Ollier
Case 8 Case 8. They can occur anywhere but most frequently involve the short tubular bones of the hands and feet. Only comments written in English can be processed. Most patients have bilateral involvement but often significant asymmetry 4. Subscribe to our Newsletter. Achondrogenesis type 2 Hypochondrogenesis.