Craniosynostosis Autosomal Dominant

Common Name(s)

Craniosynostosis Autosomal Dominant

Craniosynostosis - Autosomal Dominant is a rare disorder passed on genetically characterized by early fusion of the skull bones. Early fusion of the skull bones can lead to problems with brain development. Hence, individuals may have problems with reasoning and solving problems, as well as performing day-to-day tasks. The disorder is often diagnosed early in childhood, since the symptoms are very apparent. Signs like walking and talking late, slow mastering of basic tasks, and having difficulty remembering things may also suggest this disorder in children. Treatment is developed on a case-by-case basis and depends on the specific needs of the patient. Doctors seek help from various therapists and community services to provide support and care for families affected by intellectual disability.

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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How do you compare to others with this condition?

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Craniosynostosis Autosomal Dominant" 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 "Craniosynostosis Autosomal Dominant" 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 "Craniosynostosis Autosomal Dominant" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.