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Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives

Congenital ichthyoses are a group of hereditary disorders of keratinization that are challenging to treat. Affected individuals suffer not only from thickening of the skin but also associated complications such as growth restriction, hearing and eye complications, infections, and thermodysregulation...

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Autores principales: Lilly, Evelyn, Bunick, Christopher G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503504/
https://www.ncbi.nlm.nih.gov/pubmed/37719935
http://dx.doi.org/10.2147/CCID.S388608
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author Lilly, Evelyn
Bunick, Christopher G
author_facet Lilly, Evelyn
Bunick, Christopher G
author_sort Lilly, Evelyn
collection PubMed
description Congenital ichthyoses are a group of hereditary disorders of keratinization that are challenging to treat. Affected individuals suffer not only from thickening of the skin but also associated complications such as growth restriction, hearing and eye complications, infections, and thermodysregulation. This clinical review provides a practical roadmap to the longitudinal care of patients with ichthyosis with both general and age- and disease-specific recommendations. The allure of pathogenesis-based and targeted treatments for these monogenetic severe but orphan conditions shines bright as dermatological therapies enter a new era.
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spelling pubmed-105035042023-09-16 Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives Lilly, Evelyn Bunick, Christopher G Clin Cosmet Investig Dermatol Review Congenital ichthyoses are a group of hereditary disorders of keratinization that are challenging to treat. Affected individuals suffer not only from thickening of the skin but also associated complications such as growth restriction, hearing and eye complications, infections, and thermodysregulation. This clinical review provides a practical roadmap to the longitudinal care of patients with ichthyosis with both general and age- and disease-specific recommendations. The allure of pathogenesis-based and targeted treatments for these monogenetic severe but orphan conditions shines bright as dermatological therapies enter a new era. Dove 2023-09-11 /pmc/articles/PMC10503504/ /pubmed/37719935 http://dx.doi.org/10.2147/CCID.S388608 Text en © 2023 Lilly and Bunick. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Lilly, Evelyn
Bunick, Christopher G
Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title_full Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title_fullStr Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title_full_unstemmed Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title_short Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives
title_sort congenital ichthyosis: a practical clinical guide on current treatments and future perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503504/
https://www.ncbi.nlm.nih.gov/pubmed/37719935
http://dx.doi.org/10.2147/CCID.S388608
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