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Current Care and Investigational Therapies in Achondroplasia
PURPOSE OF REVIEW: The goal of this review is to evaluate the management options for achondroplasia, the most common non-lethal skeletal dysplasia. This disease is characterized by short stature and a variety of complications, some of which can be quite severe. RECENT FINDINGS: Despite several attem...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435778/ https://www.ncbi.nlm.nih.gov/pubmed/28224446 http://dx.doi.org/10.1007/s11914-017-0347-2 |
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author | Unger, Sheila Bonafé, Luisa Gouze, Elvire |
author_facet | Unger, Sheila Bonafé, Luisa Gouze, Elvire |
author_sort | Unger, Sheila |
collection | PubMed |
description | PURPOSE OF REVIEW: The goal of this review is to evaluate the management options for achondroplasia, the most common non-lethal skeletal dysplasia. This disease is characterized by short stature and a variety of complications, some of which can be quite severe. RECENT FINDINGS: Despite several attempts to standardize care, there is still no widely accepted consensus. This is in part due to absence of concrete data on the incidence of sudden unexplained death in infants with achondroplasia and the best investigation for ascertaining which individuals could benefit from foramen magnum decompression surgery. SUMMARY: In this review, we identify the different options of care and management for the various orthopedic, neurologic, and respiratory complications. In parallel, several innovative or drug repositioning therapies are being investigated that would restore bone growth but may also prevent complications. Achondroplasia is the most common non-lethal skeletal dysplasia. It is characterized by short stature and a variety of complications, some of which can be quite severe. Despite several attempts to standardize care, there is still no widely accepted consensus. This is in part due to absence of concrete data on the incidence of sudden unexplained death in infants with achondroplasia and the best investigation for ascertaining which individuals could benefit from foramen magnum decompression surgery. In this review, we identify the different options of care and management for the various orthopedic, neurologic, and respiratory complications. In parallel, several innovative or drug repositioning therapies are being investigated that would restore bone growth but may also prevent complications. |
format | Online Article Text |
id | pubmed-5435778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-54357782017-05-31 Current Care and Investigational Therapies in Achondroplasia Unger, Sheila Bonafé, Luisa Gouze, Elvire Curr Osteoporos Rep Rare Bone Disease (C Langman and E Shore, Section Editors) PURPOSE OF REVIEW: The goal of this review is to evaluate the management options for achondroplasia, the most common non-lethal skeletal dysplasia. This disease is characterized by short stature and a variety of complications, some of which can be quite severe. RECENT FINDINGS: Despite several attempts to standardize care, there is still no widely accepted consensus. This is in part due to absence of concrete data on the incidence of sudden unexplained death in infants with achondroplasia and the best investigation for ascertaining which individuals could benefit from foramen magnum decompression surgery. SUMMARY: In this review, we identify the different options of care and management for the various orthopedic, neurologic, and respiratory complications. In parallel, several innovative or drug repositioning therapies are being investigated that would restore bone growth but may also prevent complications. Achondroplasia is the most common non-lethal skeletal dysplasia. It is characterized by short stature and a variety of complications, some of which can be quite severe. Despite several attempts to standardize care, there is still no widely accepted consensus. This is in part due to absence of concrete data on the incidence of sudden unexplained death in infants with achondroplasia and the best investigation for ascertaining which individuals could benefit from foramen magnum decompression surgery. In this review, we identify the different options of care and management for the various orthopedic, neurologic, and respiratory complications. In parallel, several innovative or drug repositioning therapies are being investigated that would restore bone growth but may also prevent complications. Springer US 2017-02-21 2017 /pmc/articles/PMC5435778/ /pubmed/28224446 http://dx.doi.org/10.1007/s11914-017-0347-2 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Rare Bone Disease (C Langman and E Shore, Section Editors) Unger, Sheila Bonafé, Luisa Gouze, Elvire Current Care and Investigational Therapies in Achondroplasia |
title | Current Care and Investigational Therapies in Achondroplasia |
title_full | Current Care and Investigational Therapies in Achondroplasia |
title_fullStr | Current Care and Investigational Therapies in Achondroplasia |
title_full_unstemmed | Current Care and Investigational Therapies in Achondroplasia |
title_short | Current Care and Investigational Therapies in Achondroplasia |
title_sort | current care and investigational therapies in achondroplasia |
topic | Rare Bone Disease (C Langman and E Shore, Section Editors) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435778/ https://www.ncbi.nlm.nih.gov/pubmed/28224446 http://dx.doi.org/10.1007/s11914-017-0347-2 |
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