Results 171 to 180 of about 121,956 (356)

Racial Differences in Disease Characteristics of Pediatric Hidradenitis Suppurativa

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Understanding the potential racial differences in presentation, severity, and outcomes of pediatric hidradenitis suppurativa (HS) can help deliver equitable and individualized care, especially as this condition is increasingly being acknowledged in this population.
Toluwalashe Onamusi   +2 more
wiley   +1 more source

Classical Juvenile Pityriasis Rubra Pilaris Treated With Secukinumab: Case Report and a Review of Biological Treatments in the Pediatric Population

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Pityriasis rubra pilaris (PRP) is a rare, chronic papulosquamous disorder with limited treatment options in pediatric patients. We report the case of a 9‐year‐old boy with juvenile PRP (type III), who achieved complete disease remission after treatment with secukinumab, an IL‐17A inhibitor, following initial therapeutic resistance to topical ...
Zeno Fratton   +2 more
wiley   +1 more source

Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Monilethrix is a rare congenital hair disorder characterized by fragile, beaded hair shafts due to mutations in various keratin or desmoglein 4 genes. A systematic review of 24 studies (16 pediatric only, 3 mixed adult and pediatric, 3 adult only, and 2 unspecified) evaluating various treatment modalities identified topical and oral minoxidil ...
Adam C. Yu   +2 more
wiley   +1 more source

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads (PLACK) syndrome (OMIM616295) is an exceptionally rare autosomal recessive genodermatosis caused by loss‐of‐function pathogenic variants in the CAST gene, encoding calpastatin.
Fiona Haxho   +7 more
wiley   +1 more source

Infantile pustular psoriasis: Case report of successful treatment with acitretin in a 4-week-old infant

open access: yesJAAD Case Reports, 2021
Shantanu Srivatsa, MScGH   +2 more
doaj  

Low satisfaction with medical care among patients with hidradenitis suppurativa: A multicenter study

open access: yes
Journal of the European Academy of Dermatology and Venereology, EarlyView.
Kerstin Wolk   +19 more
wiley   +1 more source

A novel microcapsule composite Spherulites Peony Superior Retinol mitigates UVB‐induced skin damage in vitro and in vivo

open access: yesPhotochemistry and Photobiology, EarlyView.
This study explored the role of a novel microcapsule composite Spherulites Peony Superior Retinol (SPSR) on skin damage induced by UVB. The results of in vitro and human efficacy assays further demonstrate that SPSR is beneficial in replenishing skin hydration, promoting epidermal cell growth, soothing skin redness and sensitivity, reducing ROS ...
Jiejun Han   +6 more
wiley   +1 more source

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