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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...

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Autores principales: Walleczek, Nina-Katharina, Förster, Kristina, Seyr, Martina, Kadrnoska, Nadja, Kolar, Jennifer, Wasinger-Brandweiner, Verena, Vodopiutz, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
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.
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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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