Chromosome 1, Monosomy 1p22 p13

Common Name(s)

Chromosome 1, Monosomy 1p22 p13

Chromosome 1, monosomy 1p22 p13 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 hand defects or short stature, as well as intellectual disabilities and hearing loss. Although there is currently no cure for Chromosome 1, monosomy 1p22 p13, there are various resources to help manage the condition and treat birth defects. Doctors seek help from various therapists and community services to provide support and care for families affected by Chromosome 1, monosomy 1p22 p13.

Source: Advocacy organizations associated with the condition.

 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Chromosome 1, Monosomy 1p22 p13" for support, advocacy or research.

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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 "Chromosome 1, Monosomy 1p22 p13" 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 "Chromosome 1, Monosomy 1p22 p13" 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 "Chromosome 1, Monosomy 1p22 p13" 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.