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Can You Identify the Genodermatosis?
R, Santesteban Muruzábal +2 more
exaly +3 more sources
Dupilumab in the treatment of genodermatosis: A systematic review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2023SummaryDupilumab interferes with the signaling pathways of IL‐4 and IL‐13 and is effective in treating atopic dermatitis. Specific genodermatoses, including Netherton syndrome, epidermolysis bullosa pruriginosa, and hyper‐IgE syndrome, are Th2 skewed diseases with activation of type 2 inflammation. We performed this systematic review to investigate the
Po-Chien, Wu +5 more
openaire +2 more sources
X-linked ichthyosis: An oculocutaneous genodermatosis
Journal of the American Academy of Dermatology, 2010X-linked ichthyosis (XLI) is an X-linked recessive disorder of cutaneous keratinization with possible extracutaneous manifestations. It was first described as a distinct type of ichthyosis in 1965. XLI is caused by a deficiency in steroid sulfatase activity, which results in abnormal desquamation and a retention hyperkeratosis.
Camila Krysicka Janniger
exaly +3 more sources
Kindler syndrome: a focal adhesion genodermatosis
British Journal of Dermatology, 2009Kindler syndrome (OMIM 173650) is an autosomal recessive genodermatosis characterized by trauma-induced blistering, poikiloderma, skin atrophy, mucosal inflammation and varying degrees of photosensitivity. Although Kindler syndrome is classified as a subtype of epidermolysis bullosa, it has distinct clinicopathological and molecular abnormalities.
John S McGrath +2 more
exaly +4 more sources
Human Leukocyte Antigen in Genodermatosis
International Journal of Dermatology, 1984ABSTRACT: Tissue typing performed on the lymphocytes of 41 Patients, including: 23 patients with ichthyosis (15 of autosomal dominant and 8 of the x‐linded variety; 8 patients with tuberous sclerosis (epiloia); and 10 patients with acroder‐matitis enteropathica (AEP).
M, Amer, N, Afifi, I, Iskander, N, Diab
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