Identifying Families at Risk for OTC Deficiency Through Genealogy

Quoiden helps families trace hereditary links to OTC Deficiency, access free genetic testing, and connect with life-saving clinical trials - all through a secure, consent-driven platform.

How Quoiden Helps Families Face OTC Deficiency and Other Rare Genetic Disease

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Discover Genetic Risks

Traditional genetic testing has limits. Quoiden uses genealogy to reveal hereditary risks that testing may miss, allowing families to seek care and make informed decisions.

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Access Free Testing and Counseling

Families gain access to no-cost genetic testing and professional counseling, helping them understand results and take action with expert support. Start your free OTC Deficiency prescreening here.

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Connect with Research and Treatment

When appropriate, Quoiden securely connects families with clinical trials and emerging gene therapies, offering hope through science and community.

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Protect Your Families Privacy

Your data stays yours. Quoiden never stores genetic information - every step is consent-driven and built for complete confidentiality.

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Find Strength in Connection

Join a growing network of families, researchers, and advocates working together to raise awareness and advance care for rare genetic disorders.

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Build a Legacy of Health

Transform your family’s history into a tool for prevention and understanding,  creating a legacy of health, awareness, and shared care across generations.

Inspired by Family. Driven by Hope.

Born from personal loss, Quoiden was created after we lost Baine to a rare genetic disorder called OTC Deficiency at the age of 7. Through our family’s search for answers, we uncovered a powerful truth: genealogy can reveal hidden risks. Today, that discovery fuels a secure, lifesaving platform for families everywhere.

Frequently Asked Questions

Have questions about Quoiden, OTC deficiency, or rare genetic diseases? Our FAQ provides clear answers and helpful resources to guide you.

What is OTC Deficiency?

OTC deficiency is a genetic condition that affects the body’s ability to break down protein. When protein can’t be processed properly, ammonia builds up in the bloodstream, which can be dangerous - especially for the brain. The good news is that once identified through genetic testing, OTC deficiency can be managed with proper medical care.

What are the symptons of OTC Deficiency?

Symptoms of OTC deficiency can vary from mild to life-threatening. They may include:

   * Nausea or vomiting
    * Stomach pain
    * Headaches
    * Extreme tiredness
    * Confusion or disorientation
    * Trouble waking up
    * Coma

In severe cases, untreated OTC deficiency can lead to sudden death.

Who can be affected by OTC Deficiency?

OTC deficiency can affect anyone - babies, children, and adults of any sex. Because the condition is genetic, people can carry the gene without knowing it. Even if no one in your family has been diagnosed, you may still be at risk.

Is testing safe for infants and children?

Yes. Testing for OTC deficiency is non-invasive and completely safe.

If your baby is showing symptoms, testing should be done as soon as possible.

What does Quoiden do?

Quoiden helps families understand their risk of OTC deficiency, connect with doctors, and access genetic testing.

We also support education and clinical research - always with your full consent.

Learn more about what we do here.

Can Quoiden help assess my risk of OTC Deficiency?

Yes! Getting tested for OTC deficiency is simple:

1. Start with a short prescreen    questionnaire to see if you may be at    risk.

2. If you’re flagged as at risk, you’ll     complete a second, more detailed     questionnaire to help a doctor determine     whether testing is recommended.

3. If you qualify, you may receive free at-     home genetic testing.A cheek-swab kit      will be mailed to your home with clear,      easy-to-follow instructions.

4. Once your sample is processed, a      doctor reviews your results and      explains the next steps.

Will getting tested affect my health insurance?

No. A federal law called the Genetic Information Nondiscrimination Act (GINA) protects you. It prevents health insurers from using your genetic information to deny coverage or raise your rates.

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