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Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management
Skeletal disorders are inherited disorders with significant skeletal involvement and most of them are rare or extremely rare. Based on the clinical, radiological and genetic phenotype, the group of skeletal disorder comprises more than 450 different and highly heterogeneous disorders. In skeletal di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016795/ https://www.ncbi.nlm.nih.gov/pubmed/33689085 http://dx.doi.org/10.1007/s10354-021-00820-2 |
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author | Walleczek, Nina-Katharina Förster, Kristina Seyr, Martina Kadrnoska, Nadja Kolar, Jennifer Wasinger-Brandweiner, Verena Vodopiutz, Julia |
author_facet | Walleczek, Nina-Katharina Förster, Kristina Seyr, Martina Kadrnoska, Nadja Kolar, Jennifer Wasinger-Brandweiner, Verena Vodopiutz, Julia |
author_sort | Walleczek, Nina-Katharina |
collection | PubMed |
description | Skeletal disorders are inherited disorders with significant skeletal involvement and most of them are rare or extremely rare. Based on the clinical, radiological and genetic phenotype, the group of skeletal disorder comprises more than 450 different and highly heterogeneous disorders. In skeletal disorders rapid and precise diagnoses are urgently needed for patient care and are based on the combination of clinical, radiological and genetic analysis. Novel genetic techniques have revolutionized diagnostics and have a huge impact on counseling of patients and families. Disease-specific long-term management in a multidisciplinary healthcare team in highly specialized centers is recommended to optimize care for these patients. Here we describe a multidisciplinary postnatal approach for the diagnosis and management of patients and families with rare skeletal disorders at the Vienna Bone and Growth Center. We discuss the value of a multidisciplinary diagnostic and management approach in the postnatal setting and provide a diagnostic flowchart for rare skeletal disorders. |
format | Online Article Text |
id | pubmed-8016795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-80167952021-04-16 Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management Walleczek, Nina-Katharina Förster, Kristina Seyr, Martina Kadrnoska, Nadja Kolar, Jennifer Wasinger-Brandweiner, Verena Vodopiutz, Julia Wien Med Wochenschr Main Topic Skeletal disorders are inherited disorders with significant skeletal involvement and most of them are rare or extremely rare. Based on the clinical, radiological and genetic phenotype, the group of skeletal disorder comprises more than 450 different and highly heterogeneous disorders. In skeletal disorders rapid and precise diagnoses are urgently needed for patient care and are based on the combination of clinical, radiological and genetic analysis. Novel genetic techniques have revolutionized diagnostics and have a huge impact on counseling of patients and families. Disease-specific long-term management in a multidisciplinary healthcare team in highly specialized centers is recommended to optimize care for these patients. Here we describe a multidisciplinary postnatal approach for the diagnosis and management of patients and families with rare skeletal disorders at the Vienna Bone and Growth Center. We discuss the value of a multidisciplinary diagnostic and management approach in the postnatal setting and provide a diagnostic flowchart for rare skeletal disorders. Springer Vienna 2021-03-10 2021 /pmc/articles/PMC8016795/ /pubmed/33689085 http://dx.doi.org/10.1007/s10354-021-00820-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Main Topic Walleczek, Nina-Katharina Förster, Kristina Seyr, Martina Kadrnoska, Nadja Kolar, Jennifer Wasinger-Brandweiner, Verena Vodopiutz, Julia Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title | Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title_full | Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title_fullStr | Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title_full_unstemmed | Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title_short | Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
title_sort | rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management |
topic | Main Topic |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016795/ https://www.ncbi.nlm.nih.gov/pubmed/33689085 http://dx.doi.org/10.1007/s10354-021-00820-2 |
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