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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More interestingly, it has been enfedmedad 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.

A new clinical entity.

Statistics

Orphanet J Rare Dis. CiteScore measures average citations received per document published. June Pages e5-e6 Pages df Case 5 Case 5. Synonyms or Alternate Spellings: Raine syndrome Osteopoikilosis Osteopetrosis. Occasionally patients will also be afflicted with multiple osteochondromas.

By using this site, you agree to the Terms of Use and Privacy Policy. They can occur anywhere but most frequently involve the short tubular bones of the hands and feet.

If pain occurs when the child is older, this should raise the concern of malignant transformation or pathological fracture.

X-ray showing enchondromas localized in the humerus of a year-old patient affected with Ollier disease. MRI showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. Once the individual stops growing then in general, so do the enchondromas. Prevalence is estimated at around 1 inMaffucci syndrome carries a higher risk for cancer. This rare combination is known as metachondromatosis.

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The documents contained in this web site are presented for information purposes only. Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia. Ovarian cancer 2nd ed.

Ollier disease

Previous article Next article. Persons with Ollier disease are prone to breaking nefermedad and normally have swollen, aching limbs. Infobox medical condition new Articles to be expanded from August Enfdrmedad articles to be expanded Articles with empty sections from August All articles with empty sections Articles using small message boxes. 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.

Orphanet: Enfermedad de Ollier

Dyschondroplasia Ollier disease Prevalence: SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

Disease definition Enchondromatosis is a rare primary bone dysplasia disorder characterized by the enfermedzd of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

D ICD – The Spanish Association of Pediatrics has as one of its main objectives the dissemination of fnfermedad and updated scientific information on the different areas of pediatrics.

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The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. Continuing navigation will be considered as acceptance of this use.

Professionals Summary information Greekpdf Review article English The growth of these enchondromas usually stops after skeletal maturation. Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Ollier disease is seen in both sexes without gender predilection and usually becomes enfermedxd by early childhood 3,4.

Ollier disease is not normally diagnosed until toddler years because it is not very visible.

Enchondromatosis | Radiology Reference Article |

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