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Does anyone know of any links to information on studies done on ACM and

its incidence in families? When I first was diagnosed w/ACM, I

mentioned it to my son's pediatrician. He really didn't let on as to

how much he knew about it, but he did say he didn't think it was

hereditary.

I would really like for my son to have an MRI, because of his problems

with depression and also because of his unexplained sensorineural

hearing loss. But I have a feeling unless I go to his doctor armed with

some info, he'll say no. The poor child is having to deal with

psychiatrists and different kinds of meds, I'd really like to start at

the beginning and rule out ACM.

Thanks,

Sheila

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