French national protocol for the management of congenital ichthyosis.
Ann Dermatol Venereol
; 151(1): 103247, 2024 Mar.
Article
em En
| MEDLINE
| ID: mdl-38513308
ABSTRACT
Congenital ichthyoses (CI) comprise a heterogeneous group of monogenic genetic skin diseases characterized by diffuse scaling, often associated with skin inflammation. Diagnosis of the individual form of ichthyosis is complex and is guided by clinical expertise. CI usually has a major impact on quality of life (QOL) and thus requires lifelong treatment. To date, there are no curative therapies, although various symptomatic treatment options exist. The present protocol for the management of CI has been drawn up in accordance with the recommendations published in 2012 by the French National Authority for Health, based on a literature review, with the help and validation of members of the French network for rare skin diseases (FIMARAD). It provides a summary of evidence and expert-based recommendations and is intended to help clinicians with the management of these rare and often complex diseases.
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MEDLINE
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Ictiose Lamelar
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Idioma:
En
Ano de publicação:
2024
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Article