0
Skip to Content
Heterotaxy Connection
About Us
About Heterotaxy
Our Team
Contact
For Families
Researchers and Clinicians
Conferences
Advocacy and Fundraising
Resources
The Latest
Donate
Heterotaxy Connection
About Us
About Heterotaxy
Our Team
Contact
For Families
Researchers and Clinicians
Conferences
Advocacy and Fundraising
Resources
The Latest
Donate
Folder: About
Back
About Us
About Heterotaxy
Our Team
Contact
Folder: Our Work
Back
For Families
Researchers and Clinicians
Folder: Events and Advocacy
Back
Conferences
Advocacy and Fundraising
Resources
The Latest
Donate
For Clinicians, FHT2025 Alison Chandra 10/10/24 For Clinicians, FHT2025 Alison Chandra 10/10/24

Mitigating Infectious Risk in Heterotaxy: Vaccination and Prophylaxis

Dr. Jo Wilson reviews vaccination and antibiotic prophylaxis in the Heterotaxy population.

Read More
For Clinicians, FHT2025 Alison Chandra 10/10/24 For Clinicians, FHT2025 Alison Chandra 10/10/24

Global Assessment of Immune Function and Hyposplenism

A comprehensive review of assessment for immune function in Heterotaxy with Dr. Douglas McDonald.

Read More
FHT2025, For Families Alison Chandra 10/9/24 FHT2025, For Families Alison Chandra 10/9/24

Fever Protocols, Immunizations, and Antibiotic Prophylaxis

Learn from Dr. Douglas McDonald as we seek to understand up-to-date recommendations for immunizations and treatment protocols. This includes what, when, and why antibiotic prophylaxis is used, and considerations important when deciding to continue or discontinue treatment.

Read More
For Clinicians, FHT2024 Alison Chandra 9/2/24 For Clinicians, FHT2024 Alison Chandra 9/2/24

Immunologic Management in Heterotaxy and Asplenia/Polysplenia Syndrome

Immunologic Management in Heterotaxy and Asplenia/Polysplenia Syndrome

Read More

Get Connected

Subscribe to our mailing list to stay up to date on upcoming events, new research, and opportunities to get involved.

Subscribe

Bringing together patients, families, and clinicians to advance research, improve outcomes, and strengthen support networks, Heterotaxy Connection is committed to building a world where no one faces Heterotaxy alone.

For Families
For Researchers
For Clinicians
Newly Diagnosed?
Resources
Clinical Trials

Info

About Us
Our Team
The Latest
Contact Us

Work

Stay in the Loop

© Heterotaxy Connection 2025.
All Rights Reserved.
Privacy Policy

Financial Disclosure