نتایج جستجو برای: inherited epidermolysis bullosa

تعداد نتایج: 34966  

Journal: :Anais brasileiros de dermatologia 2012
Hiram Larangeira de Almeida Luciane Maria Alves Monteiro Fernanda Mendes Goetze Ricardo Marques e Silva Nara Moreira Rocha

In dystrophic epidermolysis bullosa, the genetic defect of anchoring fibrils leads to cleavage beneath the basement membrane and its consequent loss. A 46 year-old female patient presented blisters with a pretibial distribution associated with nail dystrophy. Her two children had hyponychia and anonychia, which affected all toe nails and the thumb, forefinger and middle finger. DNA sequencing i...

Journal: :Acta dermato-venereologica 2016
Maya El Hachem Paola Fortugno Antonio Palmeri Manuela Helmer Citterich Andrea Diociaiuti Vittoria Proto Renata Boldrini Giovanna Zambruno Daniele Castiglia

Mutations in the laminin-332 (α3Aβ3γ2) genes cause junctional epidermolysis bullosa (JEB), a recessively inherited disease characterized by blistering and altered wound repair. In addition, specific mutations that affect the N-terminus of the α3A chain cause a JEB-related non-blistering condition characterized by chronic production of granulation tissue, suggesting a critical role of this regio...

Journal: :Genetics and molecular research : GMR 2014
K J Zhu C Y Zhu Y Zhou Y M Fan

Dystrophic epidermolysis bullosa pruriginosa (DEB-Pr) is a rare subtype of dystrophic epidermolysis bullosa (DEB). This disease is characterized by severe itching, lichenoid nodules or prurigo-like lesions, and linear scarring with a predilection for the extensor limbs. Pathogenic mutations in the type VII collagen alpha 1 (COL7A1) gene have been identified. We analyzed mutations in the COL7A1 ...

Journal: :Clinical genetics 2006
B Drera D Castiglia N Zoppi R Gardella G Tadini G Floriddia N De Luca C Pedicelli S Barlati G Zambruno M Colombi

Dystrophic epidermolysis bullosa (DEB) pruriginosa (DEB-Pr) is a rare variant of DEB due to COL7A1 dominant and recessive mutations, which is characterized by severe itching and lichenoid or nodular prurigo-like lesions, mainly involving the extremities. Less than 30 patients have been described showing variable disease expression, and frequently, delayed age of onset. We report the clinical an...

Journal: :Archives of dermatology 2010
Yong Chern Kho Lesley M Rhodes Susan J Robertson John Su George Varigos Ian Robertson Peter Hogan David Orchard Dedee F Murrell

OBJECTIVE To present epidemiologic and clinical data from the Australasian Epidermolysis Bullosa (EB) Registry, the first orphan disease registry in Australia. DESIGN Observational study (cross-sectional and longitudinal). SETTING Australian private dermatology practice, inpatient ward, and outpatient clinic. PATIENTS Systematic case finding of patients with EB simplex, junctional EB (JEB...

Journal: :Anais Brasileiros de Dermatologia 2017

Journal: :Archives of Dermatology 2011

Journal: :British Journal of Dermatology 2018

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