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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Disease definition Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas olllier the metaphyses of the long bones.
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.
Olloer image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease.
Enfermedad de Ollier | Medicina Clínica
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. Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. Achondroplasia Hypochondroplasia Thanatophoric dysplasia.
Summary and related texts. Check this box if you wish to receive a copy of your message. Clinical presentation is usually with deformity and pain present only during periods of rapid growth 3,4. They can occur anywhere but most frequently involve the short tubular bones of the hands and feet.
SRJ is a prestige metric based on the idea that not all citations are the same. If involvement of the lower limbs is significant, leg length discrepancy may occur. MRI showing enchondromas localized in the lower part of the radius of a year-old enferrmedad affected with Ollier disease.
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Case 9 Case 9. If pain occurs when the child is older, this should enfermwdad the concern of malignant transformation or pathological fracture. Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution.
This page was last edited on 14 Octoberat Lippincott Williams and Wilkins. Osteochondrodysplasia Q77—Q78 From Monday to Friday from 9 a. SRJ is a prestige metric based on the idea that not all citations are the same.
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Dyschondroplasia Ollier disease Prevalence: 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.
The journal adheres to the standards of academic research publications in all aspects including peer-review and ethical principles. X-ray showing enchondromas localized in the humerus of a year-old patient affected with Ollier disease. Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic enefrmedad. One person in everyis affected.
CiteScore measures average citations eenfermedad per document published. X-ray showing calcified enchondromas localized in finger a year-old patient affected with Ollier disease. Print Send to a friend Export reference Mendeley Statistics.
Detailed information Article for general public Olliwr Imagen de la semana. Case 7 Case 7. For all other comments, please send your remarks via contact us. Are you a health professional able to prescribe or dispense drugs?
Ollier disease – Wikipedia
Previous article Next article. Health care resources for this disease Expert centres Diagnostic tests 14 Patient organisations 50 Orphan drug s 0. Case 6 Case 6.
Professionals Summary information Greekpdf Review article English A new clinical entity. Occasionally patients will also be afflicted with multiple osteochondromas.