European Cleft Gateway
Last update 03 November 2012
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			Over 500 participants attended the European Craniofacial Congress. The main topic of the Congress was clefts of the lip and/or the palate and other craniofacial anomalies connected with them […]
Since 2012 and for the next 2 years Association ALA offers to all families of children with clefts to take the opportunity and apply for financial support of speech therapy and/or orthodontic treatment for their children from 3 to 18 years […]
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| www.ala-bg.org | www.smiletrain.org | www.ecoonline.org | 
 
			The Second National Conference on Rare Diseases was held on September 2011 in Plovdiv. It took place at the Congress centre of the Novotel – Plovdiv. Dr. Youri Anastassov and Dr. Parvan Voynov attended the forum […]
The congress is an annual event organized by NPO (Association ALA has been a member of NPO since its creation). The main topic of those congresses is the issues that patient organizations face in their everyday work. This year the discussions were directed in various aspects – National programs and strategies of the Health Ministry;…
On the annual General Meeting of ALA Association on October 16, 2011 ALA members made a decision to introduce some changes in the Board Members […]
 
			Specialists from Spain are interested in the Electronic Medical Record for Facial Anomalies (EMRFA) developed by ALA and are keen to implement it in their practice. At the invitation of Val d’Hebron Hospital, Barcelona and the Spanish Society for Facial Anomalies, and through the COST project CA16234 – Inequalities in the treatment of facial anomalies…