Sixth international conference on EA n Cincinnati.

11 December 2021

The conference website 

Why an international network?

EA is a rare disease (1:2500 births) and therefore requires large cohorts from different centers/countries to improve the understanding and the knowledge of the disease and the care of the patients, to develop innovative approaches.

It is now well accepted that a multidisciplinary approach of EA including pediatric surgeons, neonatologists, geneticists, pediatric gastroenterologists, pediatric pulmonologists, general pediatricians, ENT, nutritionists, occupational therapists, speech therapists, psychologists, and specialized nurses is the most efficient in this context.

Family support groups are active in many countries and have built an international family support group federation (EAT in Europe and Australia).

Therefore, there is a need to gather all people interested and involved in the care and support of children and adults with esophageal atresia to share information and promote research in the field

The conference website 
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