top of page

R

E

S

O

U

R

C

E

S

YOU ARE NOT ALONE

One of the goals of YWHAG foundation is to support families as you navigate a new unknown. No one can better understand the pain, confusion, and weight of the diagnosis than those that have and are living it. The foundation is here to support you and we welcome you to our community. We want to help you in any way we can.

Young Volunteers

Join our Facebook YWHAG community to be connected with other families

  • Facebook

KNOWN YWHAG CASES

TOTAL COUNT - 56

26

North America

3

South America

23

Europe 

2

Africa

1

Asia

1

Australia

* Map Updated November 30, 2025

STRENGTH IN NUMBERS

The YWHAG Patient Count is the fastest way to show potential researchers and drug developers that there is a strong and connected community ready to support therapeutic development for YWHAG-related disorders.


The more individuals with confirmed YWHAG mutations we can document, the more visibility and momentum we create, making this ultra-rare condition more compelling to pharmaceutical companies, biotech partners, research institutions, clinicians, and government agencies interested in driving progress.

Firefly creative graphic showing genetic mutations. white background. orange and light blu

HAVE A QUESTION...?

Do you have questions about the YWHAG genetic mutation? For more information and quick answers, try our new virtual assistant.

RESOURCES & PUBLICATIONS

Looking for the publications and resources that were previously on this page?
Everything you need is now organized on our dedicated Publications page. Click the button below to go straight there and access all available materials and resources.

bottom of page