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.

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MRI showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia. Edit article Share article View revision history. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Support Radiopaedia and see fewer ads.

Views Read Edit View history. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. SRJ is a prestige metric based on the idea that not all citations pllier the same.

X-ray showing calcified enchondromas localized in finger a year-old patient affected with Ollier disease.

If only a few bones are involved, then little if any handicap is present, although the affected bones do have a ee rate of fracture. Case 1 Case 1. About Blog Go ad-free. Print Send to a friend Export reference Mendeley Statistics.

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X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. Nominally, the disease consists of multiple enchondromas which usually develop in childhood. Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas enferkedad the metaphyses of the long bones.

Envermedad pain occurs when the child is older, this should raise the concern of malignant transformation or pathological fracture. In distinction from solitary lesions, enchondromas of enchondromatosis are more likely to be hypercellular in nature, yet are still considered benign in the absence of other aggressive findings This page was last edited on 14 Octoberenfermedwd Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 9.

Ollier disease

This section is empty. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. 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.

The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics. The deformities are managed surgically to preserve the function ve the limb.

The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Detailed information Article for general public Svenska Summary and related texts.


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Professionals Summary information Greekpdf Review article English The etiology of enchondromatosis has been associated with post-zygote state mutations during development. Ovarian cancer 2nd ed.

Enchondromatosis | Radiology Reference Article |

CiteScore measures average citations received per document published. The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations. Log in Sign up. Previous article Next article.

The extent of disease olkier highly variable and thus so is the degree of impairment. Case 6 Case 6. Case 9 Case 9. Dyschondroplasia Ollier disease Prevalence: Achondroplasia Hypochondroplasia Thanatophoric dysplasia.

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June Pages e5-e6 Pages For all other comments, please send your remarks via contact us. The growth of these enchondromas usually stops after skeletal maturation. Health care resources for this disease Expert centres Diagnostic tests 14 Patient organisations 50 Orphan drug s 0.