HIPOACUSIA CONDUCTIVA PDF
apéndices pre-auriculares, hipoacusia conductiva o neurosensorial), malformaciones renales (malformaciones urológicas, displasia renal. Hipoacusia conductiva o de transmisión: Causada por enfermedadesuobstrucciones en el oído externo o medio, frenando el paso de las. Los dos tipos principales de pérdida auditiva son pérdida auditiva conductiva y pérdida auditiva neurosensorial. Esto se debe a que la.
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En los adultos desconocemos el porcentaje de hipoacusias hereditarias. The aim of this review is to provide conductivs updated overview of hereditary hearing loss, with special attention to the etiological diagnosis of sensorineural hearing loss, the genes most frequently mutated in our environment, the techniques available for their analysis and the clinical implications of genetic diagnosis.
In adults, the percentage of hereditary hearing conudctiva is unknown. Genetic testing is the highest yielding test for evaluating patients with sensorineural hearing loss. The process of genetic counselling is intended to inform patients and their families of the medical, psychological and familial implications of genetic diseases, as well as the risks, benefits and limitations of genetic testing.
Hipoacusias hereditarias: asesoramiento genético | Acta Otorrinolaringológica Española
The implementation of any genetic analysis must be always preceded by an appropriate genetic counselling process. Por lo tanto, los implantes cocleares suelen proporcionar un buen rendimiento en estos pacientes Por el contrario, las hipoacusias dominantes DFNA suelen ser poslinguales y progresivas. Sin embargo, existen numerosas excepciones a esta regla.
Cuando estos canales se agrupan dan lugar a las denominadas uniones tipo hendidura gap junctions. Estos pacientes se denominan heterocigotos compuestos. Puesto que el nervio auditivo funciona correctamente, los implantes cocleares en pacientes con mutaciones en el gen OTOF proporcionan un rendimiento similar al obtenido en otras hipoacusias cocleares Esto puede ocurrir como consecuencia de la elevada prevalencia en nuestro medio de portadores de mutaciones en el gen GJB2.
Tanto las deleciones como las duplicaciones de los genes previamente mencionados pueden ocasionar hipoacusias hereditarias 51,90— Read this article in English. The aim of this review is to provide an updated overview of hereditary hearing loss, with special attention to the etiological diagnosis of sensorineural hearing loss, the genes most frequently mutated in our environment, the techniques available for their analysis and the clinical implications of genetic diagnosis.
The implementation of any genetic analysis must be always preceded by an appropriate genetic counselling process. Exploring the clinical and epidemiological complexity of GJB2-linked deafness. Am J Med Genet. Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. Am J Hum Genet. Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations.
Eur J Hum Genet. Etiologic diagnosis of sensorineural hearing loss in adults.
Conductive Hearing Loss
Otolaryngol Head Neck Surg. Mutations in the Wolfram syndrome type 1 gene WFS1 define a clinical entity of dominant low-frequency sensorineural hearing loss. Arch Otolaryngol Head Neck Surg. Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene.
The implications of genetic testing for deafness. Early hearing detection and intervention: Improved diagnostic effectiveness with a sequential diagnostic paradigm in idiopathic pediatric sensorineural hearing loss. Comprehensive diagnostic battery for evaluating sensorineural hearing loss in children.
QX, a novel mutation in the gene encoding otoferlin OTOFis frequently found in Spanish patients with prelingual non-syndromic hearing loss.
De novo mutation in the gene encoding connexin GJB2 in a sporadic case of keratitis-ichthyosis-deafness KID syndrome. Am J Med Genet A. Clinical evaluation of the hearing-impaired infant. Otolaryngol Clin North Am.
Use of laboratory evaluation and radiologic imaging in the diagnostic evaluation of children with sensorineural hearing loss. Establishing the etiology of childhood hearing loss. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations. Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.
Temporal bone computed tomography findings in bilateral sensorineural hearing loss. Outcomes of clinical examination and genetic testing of individuals with hearing loss evaluated through a genetics of hearing loss clinic. Familial progressive sensorineural deafness is mainly due to the mtDNA AG mutation and is enhanced by treatment of aminoglycosides. Clinical features of patients with GJB2 connexin 26 mutations: GJB2 mutations and degree of hearing loss: Performance of cochlear implant recipients with GJB2-related deafness.
The effect of GJB2 allele variants on performance after cochlear implantation. Preservation of hearing in cochlear implant surgery: Mutation in the COCH gene is associated with superior semicircular canal dehiscence.
Correction of progressive hearing loss in superior canal dehiscence syndrome. Results of cochlear implantation in two children with mutations in the OTOF gene. Int J Pediatr Otorhinolaryngol. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Cochlear implantation in children with auditory neuropathy spectrum disorder.
Advances in molecular and cellular therapies for hearing loss. Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. Gap junctions and connexins in the inner ear: GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
Translation of “hipoacusia neurosensorial” in English
Van Naarden Braun, C. GJB2 connexin 26 variants and nonsyndromic sensorineural hearing loss: High carrier frequency of the 35delG deafness mutation in European populations. GJB2 mutations in hearing impairment: A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness Vohwinkel’s syndrome in three unrelated families.
Mutations in GJB6 cause hidrotic ectodermal dysplasia. Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss. Connexin 31 GJB3 is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment.
A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis EKV and leads to defective trafficking of the connexin 31 protein. Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx Otoferlin interacts with myosin VI: OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.
Cisd2 deficiency drives premature aging and causes mitochondria-mediated defects in mice.
Phenotype-genotype correlations in a series of wolfram syndrome families. Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.
Mutations in the seed region of human miR are responsible for nonsyndromic progressive hearing loss. An ENU-induced mutation of miR associated with progressive hearing loss in mice. X-linked deafness, stapes gushers and a distinctive defect of the inner ear. Audiological and genetic features of the mtDNA mutations. Differential diagnosis between Pendred and pseudo-Pendred syndromes: The genetic basis of long QT and short QT syndromes: Review and update of mutations causing Waardenburg syndrome.
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. Van den Ouweland, R. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Forty-six genes causing nonsyndromic hearing impairment: Molecular basis of childhood deafness resulting from mutations in the GJB2 connexin 26 gene. Diagnostic yield in the workup of congenital sensorineural hearing loss is dependent on patient ethnicity.
Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays. Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment.
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing. Genetic counselling in visual and auditory disorders. Arch Soc Esp Oftalmol. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.
N Engl J Med. Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.