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Concomitant achondroplasia and developmental dysplasia of the hip
Achondroplasia (ACH) is the most common form of hereditary dwarfism and presents with multiple musculoskeletal anomalies but is not normally associated with premature hip arthritis. Developmental dysplasia of the hip (DDH) is a spectrum of disease resulting in shallow acetabular depth and a propensi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958111/ https://www.ncbi.nlm.nih.gov/pubmed/28326385 http://dx.doi.org/10.1016/j.artd.2015.03.001 |
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author | Malcolm, Tennison L. Phan, Duy L. Schwarzkopf, Ran |
author_facet | Malcolm, Tennison L. Phan, Duy L. Schwarzkopf, Ran |
author_sort | Malcolm, Tennison L. |
collection | PubMed |
description | Achondroplasia (ACH) is the most common form of hereditary dwarfism and presents with multiple musculoskeletal anomalies but is not normally associated with premature hip arthritis. Developmental dysplasia of the hip (DDH) is a spectrum of disease resulting in shallow acetabular depth and a propensity for chronic femoral subluxation or dislocation; it is among the most common causes of premature arthritis. This case report describes the diagnosis of symptomatic DDH in a patient with ACH and highlights difficulties of primary total hip arthroplasty (THA) as a treatment option. Intraoperative radiographic imaging is advised to ensure proper prosthesis placement. Femoral osteotomy may aid visualization, reduction, and avoidance of soft tissue injury. Concomitant ACH and DDH is a challenging problem that can be successfully treated with modified THA. |
format | Online Article Text |
id | pubmed-4958111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49581112017-03-21 Concomitant achondroplasia and developmental dysplasia of the hip Malcolm, Tennison L. Phan, Duy L. Schwarzkopf, Ran Arthroplasty Today Arthroplasty in Patients with Rare Conditions Achondroplasia (ACH) is the most common form of hereditary dwarfism and presents with multiple musculoskeletal anomalies but is not normally associated with premature hip arthritis. Developmental dysplasia of the hip (DDH) is a spectrum of disease resulting in shallow acetabular depth and a propensity for chronic femoral subluxation or dislocation; it is among the most common causes of premature arthritis. This case report describes the diagnosis of symptomatic DDH in a patient with ACH and highlights difficulties of primary total hip arthroplasty (THA) as a treatment option. Intraoperative radiographic imaging is advised to ensure proper prosthesis placement. Femoral osteotomy may aid visualization, reduction, and avoidance of soft tissue injury. Concomitant ACH and DDH is a challenging problem that can be successfully treated with modified THA. Elsevier 2015-11-18 /pmc/articles/PMC4958111/ /pubmed/28326385 http://dx.doi.org/10.1016/j.artd.2015.03.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Arthroplasty in Patients with Rare Conditions Malcolm, Tennison L. Phan, Duy L. Schwarzkopf, Ran Concomitant achondroplasia and developmental dysplasia of the hip |
title | Concomitant achondroplasia and developmental dysplasia of the hip |
title_full | Concomitant achondroplasia and developmental dysplasia of the hip |
title_fullStr | Concomitant achondroplasia and developmental dysplasia of the hip |
title_full_unstemmed | Concomitant achondroplasia and developmental dysplasia of the hip |
title_short | Concomitant achondroplasia and developmental dysplasia of the hip |
title_sort | concomitant achondroplasia and developmental dysplasia of the hip |
topic | Arthroplasty in Patients with Rare Conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958111/ https://www.ncbi.nlm.nih.gov/pubmed/28326385 http://dx.doi.org/10.1016/j.artd.2015.03.001 |
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