epidermolysis


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Translations

ep·i·der·mol·y·sis

n. epidermólisis, descamación de la piel.
English-Spanish Medical Dictionary © Farlex 2012
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Drug development company RegeneRx Biopharmaceuticals Inc (OTCQB: RGRX) said on Monday that its licensee has enrolled its first patient with epidermolysis bullosa (EB) under its single-blinded, phase 2 clinical trial of the novel topically-administered drug candidate RGN-137.
(TSE 4552) has filed an application with the Ministry of Health, Labor and Welfare of Japan for additional marketing approval of TEMCELL HS Inj., allogeneic bone marrow-derived mesenchymal stem cells, for epidermolysis bullosa.
Fibrocell Science Inc., a cell and gene therapy company focused on cell-based therapies for skin and connective tissue diseases, announced the completion of a collaboration agreement with Parsippany-based Castle Creek Pharmaceuticals to develop and commercialize Fibrocell's lead gene therapy candidate, FCX-007, for the treatment of recessive dystrophic epidermolysis bullosa (RDEB), a rare, life-threatening genetic disorder diagnosed at infancy with no cure or treatment approved by the U.S.
ProQR Therapeutics announced the strategic spin out of the Dystrophic Epidermolysis Bullosa, or DEB, activities into the newly formed company, Wings Therapeutics.
Manzano shared to his fans that he received a letter this month from the parents of Miracael Macavinta, a young child who has epidermolysis bullosa.
The pair have been firm friends since 2010 when Emma, who is living with Epidermolysis bullosa or butterfly skin, won a People Of The Year Award.
Then of course there was a truly emotional moment with James Dunn winning the Outstanding Achievement Award after his battle with Epidermolysis Bullosa (EB).
After taking him to hospital in Durham, tests later revealed the youngster had a rare condition called Epidermolysis Bullosa (EB) - a genetic skin condition that causes the skin to blister and tear at the slightest touch.
Epidermolysis bullosa (EB) is an inherited, autosomal recessive, bullous disease, characterized by mucosal erosions and skin blisters.
TRANSPLANTATION of transgenic epidermal cultures successfully created a new, functional epidermis for a boy suffering from junctional epidermolysis bullosa.
Of 87 patients with bullous lesions, the most common diagnosis was pemphigus vulgaris with 36 (41.4%) patients, followed by bullous pemphigoid with 22 (25.3%) patients, dermatitis herpetiformis with 8 (9.2%) patients, pemphigus foliaceus with 6 (6.9%) patients, epidermolysis bullosa with 4 (4.6%) patients, pemphigus erythematosus with 3 (3.4%) patients and subcorneal pustular dermatosis with 1 (1.1%) patient and 7 cases had uncertain diagnoses.

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