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Targeted treatment of vascular anomalies

Vascular anomalies comprise an array of congenital developmental disorders that can lead to significant disfigurement and physiologic disarray. The vast multitude of clinical phenotypes has inherently led to misdiagnosis and patients and families enduring long diagnostic odysseys of medical care. Al...

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Detalles Bibliográficos
Autores principales: Ng, Ashley T., Tower, Richard L., Drolet, Beth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721128/
https://www.ncbi.nlm.nih.gov/pubmed/35024417
http://dx.doi.org/10.1016/j.ijwd.2021.10.014
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author Ng, Ashley T.
Tower, Richard L.
Drolet, Beth A.
author_facet Ng, Ashley T.
Tower, Richard L.
Drolet, Beth A.
author_sort Ng, Ashley T.
collection PubMed
description Vascular anomalies comprise an array of congenital developmental disorders that can lead to significant disfigurement and physiologic disarray. The vast multitude of clinical phenotypes has inherently led to misdiagnosis and patients and families enduring long diagnostic odysseys of medical care. Although the observed variation in disease manifestations remains poorly understood, targeted next-generation sequencing has pivoted our understanding of the pathobiology of vascular anomalies and, for the first time, uncovered potential pharmacologic targets for these disorders. In this review article, we highlight current and developing targeted therapies for vascular anomalies, namely phosphoinositide 3-kinase and mitogen-activated protein kinase pathway inhibitors, and discuss the future directions of targeted therapies.
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spelling pubmed-87211282022-01-11 Targeted treatment of vascular anomalies Ng, Ashley T. Tower, Richard L. Drolet, Beth A. Int J Womens Dermatol Article Vascular anomalies comprise an array of congenital developmental disorders that can lead to significant disfigurement and physiologic disarray. The vast multitude of clinical phenotypes has inherently led to misdiagnosis and patients and families enduring long diagnostic odysseys of medical care. Although the observed variation in disease manifestations remains poorly understood, targeted next-generation sequencing has pivoted our understanding of the pathobiology of vascular anomalies and, for the first time, uncovered potential pharmacologic targets for these disorders. In this review article, we highlight current and developing targeted therapies for vascular anomalies, namely phosphoinositide 3-kinase and mitogen-activated protein kinase pathway inhibitors, and discuss the future directions of targeted therapies. Elsevier 2021-11-02 /pmc/articles/PMC8721128/ /pubmed/35024417 http://dx.doi.org/10.1016/j.ijwd.2021.10.014 Text en © 2021 Published by Elsevier Inc. on behalf of Women's Dermatologic Society. https://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 Article
Ng, Ashley T.
Tower, Richard L.
Drolet, Beth A.
Targeted treatment of vascular anomalies
title Targeted treatment of vascular anomalies
title_full Targeted treatment of vascular anomalies
title_fullStr Targeted treatment of vascular anomalies
title_full_unstemmed Targeted treatment of vascular anomalies
title_short Targeted treatment of vascular anomalies
title_sort targeted treatment of vascular anomalies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8721128/
https://www.ncbi.nlm.nih.gov/pubmed/35024417
http://dx.doi.org/10.1016/j.ijwd.2021.10.014
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