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Disease at a Glance

Summary
Chromosome Xq28 duplication syndrome is a rare genetic condition. This syndrome is characterized by intellectual disability, neurobehavioral differences, and atypical facial features. The severity of the symptoms varies from person to person. Cognitive impairment is typically more severe in males. Males with the syndrome may also experience a unique combination of recurrent sinus and lung infections and allergies. Those symptoms are not usually seen in affected females. Most males with the syndrome have moderate to severe intellectual disability. Females may have milder intellectual symptoms or are unaffected. The syndrome is caused by the duplication of a specific region on the X chromosome. It is inherited in an X-linked pattern. Most individuals inherit the duplication from their mother who is often symptom-free. Some cases of new (de novo) duplications have been identified.
Summary
Chromosome Xq28 duplication syndrome is a rare genetic condition. This syndrome is characterized by intellectual disability, neurobehavioral differences, and atypical facial features. The severity of the symptoms varies from person to person. Cognitive impairment is typically more severe in males. Males with the syndrome may also experience a unique combination of recurrent sinus and lung infections and allergies. Those symptoms are not usually seen in affected females. Most males with the syndrome have moderate to severe intellectual disability. Females may have milder intellectual symptoms or are unaffected. The syndrome is caused by the duplication of a specific region on the X chromosome. It is inherited in an X-linked pattern. Most individuals inherit the duplication from their mother who is often symptom-free. Some cases of new (de novo) duplications have been identified.
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Resource(s) for Medical Professionals and Scientists on This Disease:

About Chromosome xq28 duplication syndrome

Many rare diseases have limited information. Currently, GARD aims to provide the following information for this disease:

  • Population Estimate:This section is currently indevelopment.
  • Symptoms:This section is currently in development.
  • Cause:This disease is caused by changes to the number or structure of a person’s chromosomes.
  • Organizations:Patient organizations are available to help find a specialist, or advocacy and support for this specific disease.
  • Categories:Birth DefectsGenetic DiseasesNeurological Diseases
When Do Symptoms of Chromosome xq28 duplication syndrome Begin?
This section is currently in development. 

Symptoms

This section is currently in development. 

Causes

What Causes This Disease?

Genetic Mutations

Find Your Community

How Can Patient Organizations Help?

Patient organizations can help patients and families connect. They build public awareness of the disease and are a driving force behind research to improve patients' lives. They may offer online and in-person resources to help people live well with their disease. Many collaborate with medical experts and researchers.

Services of patient organizations differ, but may include:

  • Ways to connect to others and share personal stories
  • Easy-to-read information
  • Up-to-date treatment and research information
  • Patient registries
  • Lists of specialists or specialty centers
  • Financial aid and travel resources

Please note: GARD provides organizations for informational purposes only and not as an endorsement of their services. Please contact an organization directly if you have questions about the information or resources it provides.

View GARD's criteria for including patient organizations, which can be found under the FAQs on our About page. Request an update or to have your organization added to GARD

Patient Organizations

7 Organizations

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People With

Chromosome xq28 duplication syndrome

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United States

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Chromosome xq28 duplication syndrome

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Chromosome xq28 duplication syndrome

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United Kingdom

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Participating in Clinical Studies

Clinical studies are part of clinical research and play an important role in medical advances, including for rare diseases. Through clinical studies, researchers may ultimately uncover better ways to treat, prevent, diagnose, and understand human diseases.

What Are Clinical Studies?

  1. Clinical trials determine if a new test or treatment for a disease is effective and safe by comparing groups receiving different tests/treatments.
  2. Observational studies involve recording changes over time among a specific group of people in their natural settings.
Learn more about clinical trials from this U.S. Food & Drug Administration webpage.

Why Participate in Clinical Studies?

What if There Are No Available Clinical Studies?

Join the All of Us Research Program!

What Are Clinical Studies?

Clinical studies are medical research involving people as participants. There are two main types of clinical studies:
  1. Clinical trials determine if a new test or treatment for a disease is effective and safe by comparing groups receiving different tests/treatments.
  2. Observational studies involve recording changes over time among a specific group of people in their natural settings.
Learn more about clinical trials from this U.S. Food & Drug Administration webpage.
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Why Participate in Clinical Studies?

People participate in clinical trials for many reasons. People with a disease may participate to receive the newest possible treatment and additional care from clinical study staff as well as to help others living with the same or similar disease. Healthy volunteers may participate to help others and to contribute to moving science forward.

To find the right clinical study we recommend you consult your doctors, other trusted medical professionals, and patient organizations. Additionally, you can use ClinicalTrials.gov to search for clinical studies by disease, terms, or location.
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What if There Are No Available Clinical Studies?

Join the All of Us Research Program!

ClinicalTrials.gov, an affiliate of NIH, provides current information on clinical research studies in the United States and abroad. Talk to a trusted doctor before choosing to participate in any clinical study. We recommend checking this site often and searching for studies with related terms/synonyms to improve results.
Contact a GARD Information Specialist if you need help finding more information on this rare disease or available clinical studies. Please note that GARD cannot enroll individuals in clinical studies. 
Available toll-free Monday through Friday from 12 pm to 6 pm Eastern Time
(Except: Federal Holidays)
Use the contact form to send your questions to a GARD Information Specialist.

Please allow 2 to 10 business days for us to respond.
ClinicalTrials.gov, an affiliate of NIH, provides current information on clinical research studies in the United States and abroad. Talk to a trusted doctor before choosing to participate in any clinical study. We recommend checking this site often and searching for studies with related terms/synonyms to improve results.
Contact a GARD Information Specialist if you need help finding more information on this rare disease or available clinical studies. Please note that GARD cannot enroll individuals in clinical studies. 
Available toll-free Monday through Friday from 12 pm to 6 pm Eastern Time
(Except: Federal Holidays)
Use the contact form to send your questions to a GARD Information Specialist.

Please allow 2 to 10 business days for us to respond.
Getting a Diagnosis

Take steps toward getting a diagnosis by working with your doctor, finding the right specialists, and coordinating medical care.

Last Updated: September 2024