Społeczność

CdLS World federation


The International 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 International 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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Nasze społeczności

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Dansk

Cornelia de Lange foreningen

danianorwegiaszwecjafinlandia
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English

CdLS Foundation UK & Ireland

zjednoczone królestwoirlandia
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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

hiszpania
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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

niemcyaustriaszwajcaria
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Español

Asociación Argentina del Sindrome Cornelia de Lange

argentyna
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Português

Associação Brasileira Síndrome Cornélia de Lange

brazylia
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=Português, headerIconURL=, headerTitle=Associação Brasileira Síndrome Cornélia de Lange, showHeaderStatus=true, tileStatus=[]}
Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

włochy
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=Italiano, headerIconURL=, headerTitle=Ass. Naz. di Volontariato Cornelia De Lange ONLUS, showHeaderStatus=true, tileStatus=[]}
Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

portugalia
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=Português, headerIconURL=, headerTitle=Rarissimas - Associação Nacional de Deficiências Mentais e Raras, showHeaderStatus=true, tileStatus=[]}
Nederlands

Vereniging Cornelia de Lange syndroom

niderlandybelgia
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=Nederlands, headerIconURL=, headerTitle=Vereniging Cornelia de Lange syndroom, showHeaderStatus=true, tileStatus=[]}
Français

ASSOCIATION FRANCAISE DU SYNDROME DE CORNELIA DE LANGE

francjaszwajcariabelgiaalgieria
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=Français, headerIconURL=, headerTitle=ASSOCIATION FRANCAISE DU SYNDROME DE CORNELIA DE LANGE, showHeaderStatus=true, tileStatus=[]}
Polski

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

polska
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English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

stany zjednoczone
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English

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

australianowa zelandiamalajsiafilipinysingapur
{showIcon=true, headerCSSIconClass=group-icon, serviceLabel=English, headerIconURL=, headerTitle=The Cornelia de Lange Syndrome Association (Australasia) Inc (CdLSA), showHeaderStatus=true, tileStatus=[]}
Español

Fundación CdLS COLOMBIA

kolumbia

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