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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In the original description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs. CiteScore measures average citations received per document published. Case 6 Case 6.
J Bone Joint Surg Am. SRJ is a prestige metric based on the idea that not all citations are the same. 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.
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enfermedad de Ollier – English Translation – Word Magic Spanish-English Dictionary
Are you a health professional able to prescribe or dispense drugs? As such, some authors prefer to use the term Ollier disease in cases where this distribution is present and use enchondromatosis or multiple enchondromatosis for cases where the distribution is more symmetric 5. Ollifr improve our services and products, ollire use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.
Osteochondroma osteochondromatosis Hereditary multiple exostoses.
Case 5 Case 5. The differential diagnosis for bone tumours is dependent on the age of the patient, with a very olljer set of differentials for the pediatric patient.
Spondyloepiphyseal dysplasia ollierr Multiple epiphyseal dysplasia Otospondylomegaepiphyseal dysplasia. Subscribe to our Newsletter. Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 9. 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.
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 dde of mild skeletal dysplasia in their male parents.
Are you a health professional able to prescribe or dispense drugs? Enchondromas localized in the upper part of the humerus of the same patient. Ollier disease X-ray image enfermedac enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease.
Loading Stack – 0 images remaining. Show all Show less. Summary and related texts. Case 7 Case 7. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
The etiology of enchondromatosis has been associated with post-zygote state mutations during development.
Ollier disease – Wikipedia
Support Radiopaedia and see fewer ads. This section is empty. Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia.
Thank you for updating your details. Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. Ollier disease is not normally diagnosed until toddler years because it is not very visible.
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Check this box if you wish to receive a copy of your message. X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. SRJ is a prestige metric based on the idea that not all citations are the same. 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 Synonyms or Alternate Spellings: Unable to process the form.