EN is a hamartomatous proliferation of keratinocytes. The most common dermoscopic feature of EN is large brown circles in the absence of pigment network which is similar in different histopathological variants including epidermolytic hyperkeratotic. Abstract EN is a hamartomatous proliferation of keratinocytes. The most common dermoscopic feature of EN
Ansari Mahshid Sadat +3 more
wiley +1 more source
Generalized and Naevoid Epidermolytic Ichthyosis in Denmark : Clinical and Mutational Findings [PDF]
A Danish Swedish collaboration was established to identify and classify a Danish cohort of patients with epidermolytic ichthyosis, also known as epidermolytic hyperkeratosis.
Bygum, Anette +11 more
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A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma [PDF]
We report a 6-year-old girl showing epidermolytic ichthyosis/epidermolytic hyperkeratosis (EI/EH). Targeted Next Generation Sequencing revealed a de novo, previously unidentified KRT1 mutation.
Schepis, Carmelo +4 more
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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis [PDF]
Twenty-six families with keratinopathic ichthyoses (epidermolytic ichthyosis, superficial epidermolytic ichthyosis or congenital reticular ichthyosiform erythroderma) were studied.
Schönbuchner, I. +30 more
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Linear patterns of the skin and their dermatoses
Summary Knowledge about the linear patterns of the skin is a key competence of dermatologists. Four major groups of linear patterns can be distinguished: Langer lines, dermatomes, Blaschko lines and exogenous patterns. Langer lines run in the direction of the underlying collagen fibers (least skin tension) and play an important diagnostic role for some
Sonja Senner +3 more
wiley +1 more source
Generalized epidermolytic ichthyosis with palmoplantar hyperkeratosis [PDF]
Epidermolytic ichthyosis (EI, OMIM 113800) is a rare autosomal dominant keratinization disorder that is caused by keratin 1 or 10 gene mutation. It can be classified clinically based on the presence of palmoplantar hyperkeratosis involvement and extent ...
Radiono, Sunardi +2 more
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Revised nomenclature and classification of inherited ichthyoses:Results of the First Ichthyosis Consensus Conference in Sorze 2009 [PDF]
Background: Inherited ichthyoses belong to a large, clinically and etiologically heterogeneous group of mendelian disorders of cornification, typically involving the entire integument.
Mary Williams +128 more
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Coxsackie Eruption Arising in Areas of Epidermolytic Ichthyosis
Coxsackie 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 ...
Rico, Tace, Lewis, Suzanna
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A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma [PDF]
Annular epidermolytic ichthyosis has recently been delineated as a distinct clinical phenotype within the spectrum of epidermolytic keratinization disorders.
Traupe, H. +26 more
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Hiperqueratose epidermolítica em gêmeas monozigóticas: relato de caso e revisão de literatura. [PDF]
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Sens, Mariana Mazzochi
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