A Case of Acrokeratosis Verruciformis Treated with Acitretin [PDF]
, 2009 Acrokeratosis Verruciformis is a rare autosomal dominant genodermatosis. Typically, the lesions are small, verrucous, flat papules on the dorsal aspects of the hands and feet, elbows and knees.
Ayten Ferahbaş +3 more
core
Development of erythematous scaly lesions in a cervical surgical scar [PDF]
, 2016 info:eu-repo/semantics ...
Silva, C, Torres, T.
core
Non-familial Acrokeratosis Verruciformis of Hopf [PDF]
, 2011 Acrokeratosis verruciformis of Hopf is a rare genodermatosis with an autosomal dominant mode of inheritance. It is a disorder of keratinization, characterized by multiple, flat-topped, skin-colored keratotic lesions resembling plane warts typically ...
Alain +16 more
core +2 more sources
Dermatology 2.0: Precision medicine for inflammatory skin diseases
Journal of the European Academy of Dermatology and Venereology, EarlyView.Digital immune mapping of transcriptomics profiles from inflammatory skin disease biopsies enables precise molecular diagnosis, quantification of immune modules and personalized therapy selection by matching dominant immune signatures to targeted treatments.
Jeremy Di Domizio +4 more
wiley +1 more source
LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome [PDF]
, 2017 SPINK5, encoding the putative multi-domain serine protease inhibitor LEKTI, was recently identified as the defective gene in the severe autosomal recessive ichthyosiform skin condition, Netherton syndrome (NS). Using monoclonal and polyclonal antibodies,
Al Saati, Talal +14 more
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Omalizumab for Pediatric Cutaneous Mastocytosis: Case Report and Review
Pediatric Dermatology, EarlyView.ABSTRACT We report an 11‐month‐old boy with diffuse cutaneous mastocytosis whose severe pruritus and steroid dependence resolved following off‐label treatment with omalizumab. A literature review identified five additional pediatric cases in which omalizumab led to complete symptom resolution in an average of 2 months and permitted discontinuation of ...
Janis Chang +3 more
wiley +1 more source
A Rare Clinical Presentation of Intraoral Darier's Disease
Case Reports in Pathology, 2011 Darier's disease, also known as keratosis follicularis or dyskeratosis follicularis, is a rare disorder of keratinization. It is an autosomal dominant genodermatosis with high penetrance and variable expressivity.
K. G. D. Manoja +4 more
doaj +1 more source
Mimicking Darier Disease In Vitro: A Human Epidermal Organoid Approach
Experimental Dermatology, Volume 34, Issue 12, December 2025.ABSTRACT Darier disease (DD) is a rare genetic disorder caused by mutations in the ATP2A2 gene, resulting in calcium dysregulation and impaired keratinocyte adhesion. Due to the paucity of suitable models, understanding the molecular mechanisms of DD has been challenging.
Rishika Agarwal +11 more
wiley +1 more source
Opposing Pressures of Speed and Efficiency Guide the Evolution of Molecular Machines. [PDF]
, 2019 Many biomolecular machines need to be both fast and efficient. How has evolution optimized these machines along the tradeoff between speed and efficiency?
Dill, Ken, Wagoner, Jason
core
Persistent bacterial infections, antibiotic tolerance, and the oxidative stress response [PDF]
, 2014 Certain bacterial pathogens are able to evade the host immune system and persist within the human host. The consequences of persistent bacterial infections potentially include increased morbidity and mortality from the infection itself as well as an ...
Grant, Sarah Schmidt, Hung, Deborah T.
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