46,XX Gonadal Dysgenesis Epibulbar Dermoid

Common Name(s)

46,XX Gonadal Dysgenesis Epibulbar Dermoid

46 XX gondal dysgenesis epibulbar dermoid is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This can cause birth defects such as infertility and no secondary sex characteristics, as well as epibulbar dermoid (an eye disorder), deafness, and skin tags. Although there is currently no cure for 46 XX gondal dysgenesis epibulbar dermoid, there are various resources to help manage the condition and treat birth defects. For example, surgical removal is possible for skin tags and speech therapists are helpful for individuals affected by deafness. Doctors seek help from various therapists and community services to provide support and care for families affected by 46 XX gondal dysgenesis epibulbar dermoid.

Source: Advocacy organizations associated with the condition.

 

Advocacy and Support Organizations

 

Condition Specific Organizations

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General Support Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "46,XX Gonadal Dysgenesis Epibulbar Dermoid" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "46,XX Gonadal Dysgenesis Epibulbar Dermoid" returned 0 free, full-text research articles on human participants.

Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "46,XX Gonadal Dysgenesis Epibulbar Dermoid" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.