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1.
Pediatr Dermatol ; 41(2): 263-265, 2024.
Article in English | MEDLINE | ID: mdl-38342578

ABSTRACT

This study aimed to evaluate the current management of tinea capitis in the United States, specifically focusing on patients aged 0-2 months, 2 months to 2 years, and 2 years to 18 years. An online survey, distributed through the Pediatric Dermatology Research Alliance and the Society of Pediatric Dermatology, revealed the following preferences: fluconazole for those under 2 months, griseofulvin for those aged 2 months to 2 years, and terbinafine for those aged 2 years and older. There exists inter-provider variation in tinea capitis treatment regimens within the pediatric dermatology community.


Subject(s)
Antifungal Agents , Tinea Capitis , Infant , Child , Humans , United States/epidemiology , Antifungal Agents/therapeutic use , Itraconazole , Dermatologists , Naphthalenes , Tinea Capitis/diagnosis , Tinea Capitis/drug therapy , Tinea Capitis/epidemiology , Griseofulvin/therapeutic use
2.
Cell Rep ; 28(13): 3338-3352.e6, 2019 09 24.
Article in English | MEDLINE | ID: mdl-31553905

ABSTRACT

Mucociliary epithelia provide a first line of defense against pathogens. Impaired regeneration and remodeling of mucociliary epithelia are associated with dysregulated Wnt/ß-catenin signaling in chronic airway diseases, but underlying mechanisms remain elusive, and studies yield seemingly contradicting results. Employing the Xenopus mucociliary epidermis, the mouse airway, and human airway Basal cells, we characterize the evolutionarily conserved roles of Wnt/ß-catenin signaling in vertebrates. In multiciliated cells, Wnt is required for cilia formation during differentiation. In Basal cells, Wnt prevents specification of epithelial cell types by activating ΔN-TP63, a master transcription factor, which is necessary and sufficient to mediate the Wnt-induced inhibition of specification and is required to retain Basal cells during development. Chronic Wnt activation leads to remodeling and Basal cell hyperplasia, which are reversible in vivo and in vitro, suggesting Wnt inhibition as a treatment option in chronic lung diseases. Our work provides important insights into mucociliary signaling, development, and disease.


Subject(s)
Epithelium/metabolism , Transcription Factors/genetics , Tumor Suppressor Proteins/genetics , Wnt Signaling Pathway/immunology , beta Catenin/metabolism , Animals , Cell Differentiation , Humans , Mice
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