Comunità

The World Federation of CdLS Support



The World Federation of National CdLS Support Organizations (CDLS World) is a not for profit voluntary HUB of world-wide organisations and communities united by Cornelia de Lange syndrome with one common mission to reach out, provide help and give hope.

mission

Our mission

"We are determined to contribute to an early and accurate diagnosis of the Cornelia de Lange syndrome (CdLS), to support research into aspects of the syndrome, to help people with CdLS and to parents, brothers and sisters, grandparents, families help carers and doctors to make decisions based on good information. ""

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The International Federation of National CdLS Support Organizations (CDLS World)

The World Federation of National CdLS Support Organizations (CDLS World) is a not for profit voluntary HUB of world-wide organisations and communities united by Cornelia de Lange syndrome with one common mission to reach out, provide help and give hope.
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Informazioni di contatto

Contact person: David Axtell
PO Box 8368
Ripley
Derbyshire
DE5 4DA
United Kingdom

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I nostri volontari e sostenitori...

Latin America Liaison

Paola הודיה Mannucci הראל

Council member

Gerritjan Koekkoek

Treasurer

Clare Crawford

Volunteer Spanish-speaking Communities

Andrea Morales

Chairman

David Axtell

Chair of the Care Council

Bernadette Dalingwater

Connettiti

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Le nostre comunità

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Dansk

Cornelia de Lange foreningen

danimarcanorvegiasveziafinlandia
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English

CdLS Foundation UK and Ireland

regno unitoirlanda
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

spagna
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English

Canadian CdLS Foundation

canada
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עברית

(CdLS) האגודה הישראלית תסמונת קורנליה דה לנגה

israele
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

germaniaaustriasvizzera
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Español

Comunidad Argentina del Sindrome Cornelia de Lange

argentina
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Português

Associação Brasileira Síndrome Cornélia de Lange

brasile
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Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

italia
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Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

portogallo
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Nederlands

Vereniging Cornelia de Lange syndroom

paesi bassibelgio
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Français

ASSOCIATION FRANÇAISE DU SYNDROME DE CORNELIA DE LANGE

franciasvizzerabelgioalgeria
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Polski

Stowarzyszenie Dzieci i Rodzin Cornelia de Lange Syndrom (CdLS) w Polsce

polonia
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

stati uniti
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English

The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA)

australianuova zelandamalaysiafilippinesingapore
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Español

Fundación CdLS COLOMBIA

colombia

About the website contents

All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: 

Send a email: info@cdlsWorld.org