An overview of hereditary hearing loss

YA Bayazit, M Yılmaz - Orl, 2006 - karger.com
Understanding the genetic basis of hearing loss is important because almost 50% of
profound hearing loss are caused by genetic factors and more than 120 independent genes …

Deafness genes: expressions of surprise

KP Steel, TJ Bussoli - Trends in Genetics, 1999 - cell.com
Recent rapid progress in identifying genes involved in deafness has suggested that a wide
range of different types of gene products can result in hearing impairment, which, given the …

Genetics Of Human Hereditary Hearing Impairment.

R Meena, M Ayub - Journal of Ayub Medical College, Abbottabad …, 2017 - europepmc.org
Hereditary hearing impairment is heterogeneous type of disorder which can be caused due
to environmental as well as genetical factors. Two distinct types of hereditary hearing loss …

Hearing molecules: contributions from genetic deafness

MD Eisen, DK Ryugo - Cellular and molecular life sciences, 2007 - Springer
Considerable progress has been made over the past decade identifying many genes
associated with deafness. With the identification of these hereditary deafness genes and the …

[HTML][HTML] Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss

Genetic Evaluation of Congenital Hearing Loss … - Genetics in …, 2002 - Elsevier
The advent of hearing screening in newborns in many states has led to an increase in the
use of genetic testing and related genetic services in the follow-up of infants with hearing …

Genetic causes of nonsyndromic hearing loss

ABS Giersch, CC Morton - Current opinion in pediatrics, 1999 - journals.lww.com
Explosive progress is being made in genetic studies of hearing and deafness from the
clinical and basic research perspectives. Greater than half of hearing loss is estimated to …

Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss

CM Sloan-Heggen, AO Bierer, AE Shearer, DL Kolbe… - Human genetics, 2016 - Springer
Hearing loss is the most common sensory deficit in humans, affecting 1 in 500 newborns.
Due to its genetic heterogeneity, comprehensive diagnostic testing has not previously been …

Genetics of hearing loss—nonsyndromic

KW Chang - Otolaryngologic Clinics of North America, 2015 - oto.theclinics.com
Hearing loss is the most common congenital sensory impairment, affecting 1 in 500
newborns and 1 in 300 children by the age of 4. 1 Approximately 1 in 1000 newborns has …

Genes and deafness

KP Steel, SDM Brown - Trends in Genetics, 1994 - Elsevier
Many different genes appear to be involved in the development and function of the
mammalian inner ear. Some of the genes involved during early inner ear morphogenesis …

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients

D Vozzi, A Morgan, D Vuckovic, A D'Eustacchio… - Gene, 2014 - Elsevier
Deafness is a really common disorder in humans. It can begin at any age with any degree of
severity. Hereditary hearing loss is characterized by a vast genetic heterogeneity with more …