Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yakov Pessach"'
Publikováno v:
Clinical and Experimental Dermatology. 36:406-411
Summary Background. Erythrokeratoderma variabilis (EKV) is a rare disorder of cornification usually associated with dominant mutations in the genes GJB3 and GJB4, which code for connexin (Cx)31 and Cx30.3, respectively, and contribute to the formatio
Publikováno v:
Clinical and Experimental Dermatology. 37:31-33
Chanarin-Dorfman syndrome (CDS) is an autosomal recessive metabolic disorder characterized by congenital ichthyosis and visceral complications due to accumulation of neutral lipids. CDS is caused by mutations in the ABHD5 (previously termed CGI-58) g
Autor:
Ronald Jaffe, Anat Kesler, Chezi Ganzel, Eli Sprecher, Yakov Pessach, Iris Yaish, Orna Aizenstein, Ilan Goldberg, Iris Eshed, Mirra Manevich-Mazor, Yehuda Shoenfeld, Roei D Mazor, Alexander Gural
Publikováno v:
BMC Medicine
Background Erdheim-Chester Disease (ECD), a non Langerhans’ cell histiocytosis of orphan nature and propensity for multi-systemic presentations, comprises an intricate medical challenge in terms of diagnosis, treatment and complication management.
Publikováno v:
Clinical and Experimental Dermatology.
Reactive angioendotheliomatosis (RAE) is a diagnostically challenging condition characterized by multiple possible clinical presentations, which makes diagnosis challenging. We present a rare case of RAE mimicking cellulitis in a 74-year-old woman wi
Publikováno v:
Anticancer research. 29(5)
In view of several studies highlighting an observation of an erythematous eruption in the vicinity of or distant from the lesion in melanoma patients (The Brenner sign), this study sought to assess whether this phenomenon might be related to the bloo