Development of hip dysplasia in hereditary multiple exostosis
In approximately 25% of patients with hereditary multiple exostosis, there is an abnormal osteochondral formation localized in the femoral proximal metaphysis. This formation often causes a mechanically progressive insufficiency of the acetabular cavity, a true developmental hip dysplasia, that toge...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2001
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22420
- Acceso en línea:
- https://doi.org/10.1097/01241398-200103000-00014
https://repository.urosario.edu.co/handle/10336/22420
- Palabra clave:
- Article
Cancer surgery
Child
Chondroma
Clinical article
Female
Genetic counseling
Hereditary multiple exostosis
Hip disease
Hip dysplasia
Human
Hyperostosis
Male
Osteochondroma
Priority journal
Coxa valga
Developmental dysplasia
Ext gene family
Femur-hip osteochondroma
Hereditary multiple exostosis
Hip
- Rights
- License
- Abierto (Texto Completo)
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5cefaa73-bf47-459e-8329-b62bb42af834-12020-05-25T23:56:25Z2020-05-25T23:56:25Z2001In approximately 25% of patients with hereditary multiple exostosis, there is an abnormal osteochondral formation localized in the femoral proximal metaphysis. This formation often causes a mechanically progressive insufficiency of the acetabular cavity, a true developmental hip dysplasia, that together with a coxa valga deformity, which is also present, causes a gradual deterioration in the relations of this joint. This malformation has a poor prognosis and is difficult to manage. Although this entity is rather frequent and quite severe, it is rarely found in the medical literature. The author describes six private cases, taken from a total of 24,000 patients (0.25/1000) as examples of this entity, and provides a review of the literature.application/pdfhttps://doi.org/10.1097/01241398-200103000-000141539257002716798https://repository.urosario.edu.co/handle/10336/22420engLippincott Williams and Wilkins211No. 2205Journal of Pediatric OrthopaedicsVol. 21Journal of Pediatric Orthopaedics, ISSN:15392570, 02716798, Vol.21, No.2 (2001); pp. 205-211https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035119756&doi=10.1097%2f01241398-200103000-00014&partnerID=40&md5=9b54328135faede1ca1025beef0774fcAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURArticleCancer surgeryChildChondromaClinical articleFemaleGenetic counselingHereditary multiple exostosisHip diseaseHip dysplasiaHumanHyperostosisMaleOsteochondromaPriority journalCoxa valgaDevelopmental dysplasiaExt gene familyFemur-hip osteochondromaHereditary multiple exostosisHipDevelopment of hip dysplasia in hereditary multiple exostosisarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Malagón V.10336/22420oai:repository.urosario.edu.co:10336/224202022-05-02 07:37:14.156038https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Development of hip dysplasia in hereditary multiple exostosis |
title |
Development of hip dysplasia in hereditary multiple exostosis |
spellingShingle |
Development of hip dysplasia in hereditary multiple exostosis Article Cancer surgery Child Chondroma Clinical article Female Genetic counseling Hereditary multiple exostosis Hip disease Hip dysplasia Human Hyperostosis Male Osteochondroma Priority journal Coxa valga Developmental dysplasia Ext gene family Femur-hip osteochondroma Hereditary multiple exostosis Hip |
title_short |
Development of hip dysplasia in hereditary multiple exostosis |
title_full |
Development of hip dysplasia in hereditary multiple exostosis |
title_fullStr |
Development of hip dysplasia in hereditary multiple exostosis |
title_full_unstemmed |
Development of hip dysplasia in hereditary multiple exostosis |
title_sort |
Development of hip dysplasia in hereditary multiple exostosis |
dc.subject.keyword.spa.fl_str_mv |
Article Cancer surgery Child Chondroma Clinical article Female Genetic counseling Hereditary multiple exostosis Hip disease Hip dysplasia Human Hyperostosis Male Osteochondroma Priority journal Coxa valga Developmental dysplasia Ext gene family Femur-hip osteochondroma Hereditary multiple exostosis Hip |
topic |
Article Cancer surgery Child Chondroma Clinical article Female Genetic counseling Hereditary multiple exostosis Hip disease Hip dysplasia Human Hyperostosis Male Osteochondroma Priority journal Coxa valga Developmental dysplasia Ext gene family Femur-hip osteochondroma Hereditary multiple exostosis Hip |
description |
In approximately 25% of patients with hereditary multiple exostosis, there is an abnormal osteochondral formation localized in the femoral proximal metaphysis. This formation often causes a mechanically progressive insufficiency of the acetabular cavity, a true developmental hip dysplasia, that together with a coxa valga deformity, which is also present, causes a gradual deterioration in the relations of this joint. This malformation has a poor prognosis and is difficult to manage. Although this entity is rather frequent and quite severe, it is rarely found in the medical literature. The author describes six private cases, taken from a total of 24,000 patients (0.25/1000) as examples of this entity, and provides a review of the literature. |
publishDate |
2001 |
dc.date.created.spa.fl_str_mv |
2001 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:56:25Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:56:25Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1097/01241398-200103000-00014 |
dc.identifier.issn.none.fl_str_mv |
15392570 02716798 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22420 |
url |
https://doi.org/10.1097/01241398-200103000-00014 https://repository.urosario.edu.co/handle/10336/22420 |
identifier_str_mv |
15392570 02716798 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
211 |
dc.relation.citationIssue.none.fl_str_mv |
No. 2 |
dc.relation.citationStartPage.none.fl_str_mv |
205 |
dc.relation.citationTitle.none.fl_str_mv |
Journal of Pediatric Orthopaedics |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 21 |
dc.relation.ispartof.spa.fl_str_mv |
Journal of Pediatric Orthopaedics, ISSN:15392570, 02716798, Vol.21, No.2 (2001); pp. 205-211 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035119756&doi=10.1097%2f01241398-200103000-00014&partnerID=40&md5=9b54328135faede1ca1025beef0774fc |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Lippincott Williams and Wilkins |
institution |
Universidad del Rosario |
dc.source.instname.spa.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1814167738740899840 |