Mosaic variegated aneuploidy syndrome 2

Common Name(s)

Mosaic variegated aneuploidy syndrome 2

Mosaic variegated aneuploidy syndrome is an autosomal recessive disorder characterized by poor growth and variable phenotypic manifestations, such as facial dysmorphism and congenital heart defects, associated with mosaic aneuploidies resulting from defects in cell division (summary by {4:Snape et al., 2011}). See also MVA1 ({257300}), caused by mutation in the BUB1B gene ({602860}) on chromosome 15q15.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Mosaic variegated aneuploidy syndrome 2" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.