Results 161 to 170 of about 1,421 (196)
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Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis)
British Journal of Dermatology, 1994To evaluate the role of filaggrin in keratin filament aggregation in epidermolytic ichthyosis (epidermolytic hyperkeratosis, EH), we studied EH skin by light and electron microscopic immunohistochemistry, and biochemical analysis using sodium dodecylsulphate-polyacrylamide gel electrophoresis and immunoblotting.
A, Ishida-Yamamoto +4 more
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Annular epidermolytic ichthyosis: A unique phenotype
Journal of the American Academy of Dermatology, 1992A 30-year-old white woman developed bullous and ichthyosiform skin lesions at the age of 8 months. Blistering ceased at puberty, but the hyperkeratotic plaques persisted. She subsequently delivered five children, two of whom were affected with a bullous type of ichthyosis.
E E, Sahn, C E, Weimer, P D, Garen
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Management of Epidermolytic Ichthyosis in the Newborn
Neonatal Network, 2016AbstractEpidermolytic ichthyosis (EI) is a rare autosomal dominant genodermatosis that presents at birth as a bullous disease, followed by a lifelong ichthyotic skin disorder.1 Essentially, it is a defective keratinization caused by mutations of keratin 1 (KRT1) or keratin 10 (KRT10) genes, which lead to skin fragility, blistering, and eventually ...
Mondell, Avril, Cheryl, Riley
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Superficial Epidermolytic Ichthyosis: A Report of Two Families
Pediatric Dermatology, 2012Abstract: Superficial epidermolytic ichthyosis (SEI), previously known as ichthyosis bullosa of Siemens, is a rare genetic skin condition, characterized by blisters and hyperkeratosis. It can be easily confused with epidermolytic hyperkeratosis, known now as epidermolytic ichthyosis, and genetic testing can be helpful in differentiating between the ...
Tessa, Cervantes +2 more
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Coxsackie Eruption Arising in Areas of Epidermolytic Ichthyosis
Pediatric Dermatology, 2015AbstractCoxsackie eruptions concentrated in areas of atopic dermatitis, a phenomenon termed “eczema coxsackium,” has been well described in the literature but, to our knowledge, the concentration of coxsackie viral lesions to areas of ichthyosis has not been reported.
Lewis, Suzanna, Rico, Tace
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Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
Pediatric Dermatology, 2016AbstractSuperficial epidermolytic ichthyosis (SEI) is an autosomal dominant disorder caused by a mutation in the keratin 2 gene and clinically characterized by mild hyperkeratosis, superficial blisters and shedding, referred to as the moulting phenomenon. We report a case of SEI in an 18‐month‐old girl presenting with marked hypertrichosis.
Ana, Gameiro +3 more
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Ichthyosis bullosa of Siemens: A unique type of epidermolytic hyperkeratosis
Journal of the American Academy of Dermatology, 1986We report the second family of ichthyosis bullosa, an entity that was first described by Siemens in 1937 and since then has fallen into oblivion. Clinically, ichthyosis bullosa is characterized by blistering resembling epidermolysis bullosa simplex and by generalized, yet circumscribed dark gray hyperkeratoses covering mainly the arms and the legs ...
H, Traupe, G, Kolde, H, Hamm, R, Happle
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Epidermolytic Ichthyosis in a Neonate
The Journal of Pediatrics, 2023Sharon, Pan +3 more
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Exploring TH17-mediated inflammation in epidermolytic ichthyosis: Clinical and mechanistic insight
Clinical ImmunologyEpidermolytic ichthyosis (EI) is a genetic skin disorder caused by mutations in the KRT1 and KRT10 genes, leading to severe skin abnormalities and inflammation. Current treatment options are limited, emphasizing the need for pathogenesis-based therapies.
Yidong, Tan +10 more
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