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  • We join the International Awareness Day for Rare Diseases and consolidate our relationship with CIBERER

    Posted by Piel de Mariposa on 2 March, 2020

    Today, 29th of February 2020, we join the campaign created by the Spanish Federation for rare diseases (FEDER) “Our hope grows with you” to celebrate world awareness day for…


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  • An exciting breakthrough in a new skin regeneration treatment

    Posted by Piel de Mariposa on 7 May, 2019

    50% of the people in Spain with dystrophic recessive Epidermolysis bullosa (EB) share the same genetic mutation in a very specific gene.  The consequence of this mutation is that the collagen protein does not develop correctly.  This affects the skin structure and the…


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The DEBRA Butterfly Children's Charity is an organisation which exists specifically to help people with Epidermolysis Bullosa. A non profit organisation dedicated to improving the lives of people with EB and their families in Spain.

CONTACT US

Debra Piel de Mariposa
C/ Jacinto Benavente Nº 12
29601 Marbella (Málaga)

Tlfno:(+34) 952 816 434    info@debra.es

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