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Universal neonatal hearing screening (UNHS), which is part of early hearing detection and intervention (EHDI) programmes, refer to those services aimed at screening hearing of all newborns, regardless of the presence of a risk factor for hearing loss. UNHS is the first step in the EHDI program which indicates whether a newborn requires further ...
From 1993 to 1996, NCHAM directed a National Consortium for Newborn Hearing Screening that resulted in over 100 hospitals in 10 states implementing newborn hearing screening programs. [ 9 ] [ 10 ] [ 11 ] From 1996 to 2000, NCHAM staff worked with newborn hearing screening programs in 35 states and provided direct assistance to over 200 ...
In X-linked hearing loss, the mother carries the recessive trait for hearing loss on the sex chromosome. She can pass on the trait to male and female children, but usually only male children are affected. There are some genetic syndromes, in which hearing loss is one of the known characteristics.
The Early Hearing Detection Intervention (EHDI) mandates each state and territory in the United States to implement programs providing newborn screening, diagnostic and early intervention. Programs are publicly funded and provided for free or at reduced cost for any eligible child. This serves all children with hearing loss.
Newborn screening programs initially used screening criteria based largely on criteria established by JMG Wilson and F. Jungner in 1968. [6] Although not specifically about newborn population screening programs, their publication, Principles and practice of screening for disease proposed ten criteria that screening programs should meet before being used as a public health measure.
Auditory neuropathy is sometimes difficult to catch right away, even with these precautions in place. Parental suspicion of a hearing loss is a trustworthy screening tool for hearing loss, too; if it is suspected, that is sufficient reason to seek a hearing evaluation from an audiologist. [10]
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