Other studies have found "no statistically significant average difference between left and right ears for average values of TOAE (transitory otoacoustic emissions) response amplitude with no contralateral acoustic stimulation in patients with Alport's syndrome. (Abreu Alves & al, 2008)"
Auditory brainstem response results for Alport Syndrome patients indicate the cochlea as the site of damage, with dramatic alterations of the stria vascularis.
Hearing loss from Alport Syndrome complications is usually permanent. Recommendations for patients include: urine testing alongside SNHL testing; otologist involvement at all stages of treatment once hearing loss presents; counseling and education to enhance coping skills; instruction for lip reading and sign language; use of hearing protection in noisy environments; and hearing aid prescription.
References
Alport Syndrome Foundation, s. (2010). What is Alport Syndrome? Retrieved 12 5, 2010, from www.alportsyndrome.org: http://www.alportsyndrome.org/what-is-alport-syndrome/
Favor, J., Gloeckner,...
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Chicoine also cautions that whenever a patient declines in function, a thorough evaluation is necessary "to look for reversible causes, or, if no reversible cause is found, to confirm that the decline is consistent with Alzheimer's disease" (Chicoine pp). In other words, just as in the general population, Alzheimer's disease is a diagnosis of exclusion in persons with Down's (Chicoine pp). Because traditional neuropshychological testing, such as used for
So, they are saying that the initial screening followed with a second round of screening have proved to have a detection rate as high as 84%, the article continues. Also, integrated screening (combining the results of tests in the first and second-trimesters) has also proved to be valuable in terms of detection of DS during pregnancy. The problem with integrated screening, the article points out, is that there is quite
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