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Associação Brasileira Síndrome Cornélia de Lange

A Síndrome de Cornélia de Lange, mais conhecida como CDLS é um distúrbio genético presente desde o nascimento.

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Associação Brasileira Síndrome Cornélia de Lange

A Síndrome de Cornélia de Lange, mais conhecida como CDLS é um distúrbio genético presente desde o nascimento.

Participates in the The World Federation of CdLS Support

Supports

Contact information

MEMBROS DIRETORIA EXECUTIVA

Fábio Alves

Diretor Presidente

Tatiana Arantes Alves

Vice Diretora Presidente

Arlete La Selva

Diretora Clínica

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Otherwise contact your national centre of expertise

Network of experts for Associação Brasileira Síndrome Cornélia de Lange

Network of expertise

International Scientific Advisory Council (SAC)

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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

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English

CdLS Foundation UK and Ireland

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Español

Asociación Española Síndrome de Cornelia de Lange (AESCdL)

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English

Canadian CdLS Foundation

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עברית

(CdLS) האגודה הישראלית תסמונת קורנליה דה לנגה

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Deutsch

Arbeitskreis Cornelia de Lange Syndrom e.V.

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Español

Comunidad Argentina del Sindrome Cornelia de Lange

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Português

Associação Brasileira Síndrome Cornélia de Lange

Italiano

Ass. Naz. di Volontariato Cornelia De Lange ONLUS

Português

Rarissimas - Associação Nacional de Deficiências Mentais e Raras

Nederlands

Vereniging Cornelia de Lange syndroom

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Français

ASSOCIATION FRANÇAISE DU SYNDROME DE CORNELIA DE LANGE

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Polski

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

English

the Cornelia de Lange Syndrome (CdLS) Foundation USA

English

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

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Español

Fundación CdLS 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

Associação Brasileira Síndrome Cornélia de Lange

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Associação Brasileira Síndrome Cornélia de Lange

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