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I would go to chargesyndrome.org website. Contact someone there and they can give you the information you are wanting.

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15y ago

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Charge syndrome is genetic. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. This syndrome is a common cause of congenital anomalies affecting several tissues in nonrandom fashion. Some research has been shown that detected mutations are in the gene CHD7 in 10 of 17 individuals with CHARGE syndrome that didn't have microdeletions, accounting for the disease in most affected individuals.


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On the Charge Syndrome website, is a page that speaks about a charity that funds and takes care of families with children that have CHARGE syndrome and information about how it does so, and for what reasons.


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