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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Lippincott Williams and Wilkins. The Impact Factor measures dee average number of citations received in a particular year by papers published in the journal during the two receding years.

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Case 9 Case 9. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

Subscribe to our Newsletter. Occasionally patients will also be afflicted with multiple osteochondromas. 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. Case 7 Case 7. One person in everyis affected.

If pain occurs when the child is older, this should raise the concern of malignant transformation or pathological fracture. Re continua navegando, consideramos que acepta su uso. On radiographs, streaks of low density are seen projecting through the diaphyses into the epiphyses of the long bones, due to ectopic cartilage deposits. This rare combination is known as metachondromatosis. Case 6 Case 6. From Monday to Friday from 9 a. D ICD – SRJ is a prestige metric based on the idea that not all citations are the same.


Dyschondroplasia Ollier disease Prevalence: Are you a health professional able enfemedad prescribe or dispense drugs?

enfermedad de Ollier – English Translation – Word Magic Spanish-English Dictionary

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. More interestingly, it has been reported that the PTHrP parathyroid hormone-related protein receptor 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.

Health care resources for this disease Expert centres Diagnostic tests 14 Patient organisations 50 Orphan drug s 0. Check this box if you wish to receive a copy of your message. Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. Once the individual stops growing then in general, so do the enchondromas. Most patients have bilateral involvement but often significant asymmetry 4. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia. Multiple enchondromatosis, Ollier disease.

They can occur anywhere but most frequently involve the short tubular bones of the hands and feet. Edit article Share article View revision history. Other search option s Alphabetical list. This page was last edited on 14 Octoberat Ollier disease is not normally diagnosed until toddler years because it is not very visible. Print Send to a friend Export ollieg Mendeley Statistics.


Unable to process the form. Detailed information Article for general public Svenska The deformities are managed surgically to preserve the function of the limb. Orphanet J Rare Dis.

Ollier disease

Nominally, the disease consists of multiple enchondromas which usually develop in childhood. This item has received.

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Ollier disease X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease. If involvement of the lower limbs is significant, leg length discrepancy may occur. Log in Sign up. Spondyloepiphyseal dysplasia congenita Multiple epiphyseal dysplasia Otospondylomegaepiphyseal dysplasia. Loading Stack – 0 images remaining. You can help by adding to it. Retrieved from ” https: Continuing navigation will be considered as acceptance of this use.