Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.
نویسندگان
چکیده
منابع مشابه
Alu-mediated large deletion of the CDSN gene as a cause of peeling skin disease.
Peeling skin disease (PSD) is an autosomal recessive skin disorder caused by mutations in CDSN and is characterized by superficial peeling of the upper epidermis. Corneodesmosin (CDSN) is a major component of corneodesmosomes that plays an important role in maintaining epidermis integrity. Herein, we report a patient with PSD caused by a novel homozygous large deletion in the 6p21.3 region enco...
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متن کاملPeeling skin syndrome.
To cite: Bansal M, Mahajan S, Sankhwar S, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015210902 DESCRIPTION A 30-year-old man born of a non-consanguineous marriage presented with asymptomatic peeling of skin throughout his body, sparing palms and soles, since birth. There was no preceding history of redness or fluid-filled lesions over the affected are...
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ورودعنوان ژورنال:
- Acta dermato-venereologica
دوره 95 8 شماره
صفحات -
تاریخ انتشار 2015