קהילה

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. ""

לוח האירועים שלנו   

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.
Supports multiple communities
Supports
un

Contact information

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

Read more about our community...

המתנדבים והתומכים שלנו...

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

להתחבר

בצע את השלבים הבאים...

אחרת פנה למרכז המומחיות הלאומי שלך

Network of experts for The World Federation of CdLS Support


Collaboration helps....

Collaborating with other family communities offers shared knowledge, advocacy strength, pooled resources, and accelerated research progress. Together, these collaborations empower individuals, amplify voices, advance treatments, and raise awareness, ultimately driving positive change.

See our current partners below

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Dansk

Cornelia de Lange foreningen

דנמרקנורווגיהשוודיהפינלנד
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English

CdLS Foundation UK and Ireland

הממלכה המאוחדתאירלנד
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

ספרד
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English

Canadian CdLS Foundation

lblflagcanada
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עברית

(CdLS) האגודה הישראלית תסמונת קורנליה דה לנגה

ישראל
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

גרמניהאוסטריהשוויץ
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Español

Comunidad Argentina del Sindrome Cornelia de Lange

ארגנטינה
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Português

Associação Brasileira Síndrome Cornélia de Lange

ברזיל
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Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

איטליה
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Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

פורטוגל
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Nederlands

Vereniging Cornelia de Lange syndroom

הולנדבלגיה
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Français

ASSOCIATION FRANÇAISE DU SYNDROME DE CORNELIA DE LANGE

צרפתשוויץבלגיהאלג'יריה
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Polski

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

פלין
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

ארצות הברית
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English

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

אוסטרליהניו זילנדמלזיההפיליפיניםסינגפור
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Español

Fundación CdLS COLOMBIA

קולומביה

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