Potential treatments for genetic hearing loss in humans: current conundrums

Genetic defects are a major cause of hearing loss in newborns. Consequently, hearing loss has a profound negative impact on human daily living. Numerous causative genes for genetic hearing loss have been identified. However, presently, there are no truly curative treatments for this condition. There...

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Veröffentlicht in:	Gene therapy 2015-08, Vol.22 (8), p.603-609
Hauptverfasser:	Minoda, R, Miwa, T, Ise, M, Takeda, H
Format:	Artikel
Sprache:	eng
Schlagworte:	42/44 631/208/200 631/208/2489/201/2110 64/60 692/699/375 692/700/565/201 9/10 Animals Antisense oligonucleotides Biomedical and Life Sciences Biomedicine Care and treatment Cell Biology Childhood Deafness Ear, Inner - anatomy & histology Ear, Inner - growth & development Embryos Gene Expression Gene Therapy Genes Genetic aspects Genetic Diseases, Inborn - genetics Genetic Diseases, Inborn - therapy Genetic disorders Genetic Therapy Health aspects Hearing loss Hearing Loss - genetics Hearing Loss - therapy Hearing protection Human Genetics Humans Medical schools Nanotechnology Neonates Newborn infants Oligonucleotides, Antisense - therapeutic use review Surgery
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