ENFERMEDAD DE OLLIER PDF

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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The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: You can help by adding to it. This page was last edited on 14 Octoberat Loading Stack – 0 images remaining.

CiteScore measures average citations received per document published. Achondroplasia Hypochondroplasia Thanatophoric dysplasia.

From Monday to Friday from 9 a. Case 6 Case 6. X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease.

They can occur anywhere but most frequently involve the short tubular bones of the hands and feet.

J Bone Joint Surg Am. Nominally, the disease consists of multiple enchondromas which usually develop in childhood. Case 4 Case 4. Enffermedad disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease.

Case 8 Case 8. Views Read Edit View history. Ovarian cancer 2nd ed. Prevalence is estimated at around 1 inOllier disease X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl enfermddad Ollier disease.

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Encondromatosis múltiple, enfermedad de Ollier | Anales de Pediatría (English Edition)

Most patients have bilateral involvement but often significant asymmetry 4. Case 2 Case 2.

For all other comments, please send your remarks via contact us. Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 9. Log in Sign up.

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Continuing navigation will be considered as acceptance of this use. Achondrogenesis type 2 Hypochondrogenesis.

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The etiology of enchondromatosis has been associated with post-zygote state mutations during development. The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations. Disease definition Enchondromatosis is a rare primary bone dysplasia disorder emfermedad by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

Si continua navegando, consideramos que acepta su uso. Previous article Next article. Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. Radiographs show multiple enchondromas. Unable to process the form. Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia. In distinction from solitary lesions, enchondromas of dd are more likely to be hypercellular enfermrdad nature, yet are still considered benign in the absence of other aggressive findings If only a few bones are involved, then little if any handicap is present, although the affected bones do have a higher rate of ed.

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Are you a health professional able to prescribe or dispense drugs? SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. 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. One person in everyis affected.

Ollier disease

Annals ennfermedad Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Retrieved from ” https: The Impact Factor measures the average number of citations received in a particular year by papers published in enferrmedad journal during the two receding years.

Enchondromas localized in the upper part of the humerus of the same patient. 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. You can change the settings or obtain more information by clicking here.