Chromosome 10, Monosomy 10q

Common Name(s)

Chromosome 10, Monosomy 10q

Chromosome 10, monosomy 10q, also known as distal monosomy 10q, occurs when there is a deletion of the long arm of chromosome 10. Symptoms associated with this disorder include delayed physical and mental development as well as other abnormalities such as microcephaly, congenital heart defects, and hypotonia. Diagnosis is made by molecular analysis. 40 cases have been documented in literature so far.

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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 "Chromosome 10, Monosomy 10q" 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 10, Monosomy 10q" 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 10, Monosomy 10q" 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.