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A range of SLC26A4 variants without a common recurrent mutation underlies SLC26A4-related hearing loss in Turkey, Iran, and Mexico.
a later onset of hearing loss is usually related to EVA, in absence of SLC26A4 gene mutations
A novel SLC26A4 point mutation is associated with enlarge vestibular aqueduct syndrome.
results demonstrate that 19.2% patients with nonsyndromic deafness were caused by mutations in three common deafness genes (GJB2 (zeige GJB2 ELISA Kits), SLC26A4 and 12S rRNA) in our northern China patient group
we hypothesize that SLC26A4 coding mutations are genetic causes for nonsyndromic hearing impairment in patients bearing heterozygous GJB2 (zeige GJB2 ELISA Kits) 35delG mutations.
Ears with EVA and zero or one mutant allele of SLC26A4 have less severe hearing loss, no difference in prevalence of fluctuation, and a lower prevalence of cochlear implantation in comparison to ears with two mutant alleles of SLC26A4.
These studies implicate the involvement of pendrin-facilitated chloride-bicarbonate exchange in the regulation of airway surface liquid volume and suggest the utility of pendrin inhibitors in inflammatory lung diseases.
data suggest that many patients with SLC26A4 mutations have significant residual hearing at birth, and that the hearing deterioration in these patients occurs before 3 years of age. After age 3 years, the residual hearing was relatively stable and did not tend to deteriorate
Familial enlarged vestibular aqueduct can demonstrate a variety of atypical segregation patterns. Pseudodominant inheritance of SLC26A4 mutations or recessive alleles of other hearing loss genes may be more likely to occur in families in which deaf individuals have intermarried.
The prevalence of SLC26A4 pathogenic variants was 4% among studied Chinese patients with congenital hypothyroidism. Our study expanded the SLC26A4 mutation spectrum, provided the best estimation of SLC26A4 mutation rate for Chinese CH patients and indicated the rarity of Pendred syndrome as a cause of congenital hypothyroidism.
Study showed that early re-induction of Slc26a4 expression can prevent fluctuation of hearing in our Slc26a4-insufficient mouse model. Restoration of SLC26A4 expression and function could reduce or prevent fluctuation of hearing in enlargement of the vestibular aqueduct patients.
decreased plasma K(+) levels promote pendrin induction by aldosterone, which, in concert with Na(+)-Cl(-) cotransporter (zeige SLC12A3 ELISA Kits), counteracts the progression of hypokalemia but promotes hypertension in primary aldosterone excess.
The strial dysfunction and degeneration are the primary causes of irreversible progressive hearing loss in our Slc26a4-insufficient mouse model of vestibular aqueduct syndrome.
The Role of Epithelial Sodium Channel ENaC (zeige SCNN1A ELISA Kits) and the Apical Cl-/HCO3- Exchanger Pendrin in Compensatory Salt Reabsorption in the Setting of Na-Cl Cotransporter (NCC (zeige SLC12A3 ELISA Kits)) Inactivation.
Pendrin is expressed in the adrenal medulla, where it blunts stress-induced catecholamine release.
Pendrin gene ablation reduced ENaC (zeige SCNN1A ELISA Kits)-mediated Na(+) absorption by reducing channel open probability as well as by reducing channel density through changes in subunit total protein abundance and subcellular distribution.
The result provides insight into the role of Na+ transport in the development and regulation of endolymphatic hydrops due to pendrin mutations.
Insufficient availability of thyroid hormone (zeige PTH ELISA Kits) during inner ear development plays an important role in the mechanism underlying deafness as a result of SLC26A4 mutations.
Together these data suggest that pertussis toxin contributes to pertussis pathology through the upregulation of pendrin, which promotes conditions favoring inflammatory pathology.
Using a transgenic mouse line in which all Slc26a4 expression was under the control of doxycycline, showed that fluctuations of hearing result from fluctuations of endocochlear potential and stria vascularis dysfunction in Slc26a4-insufficient mouse ears
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene\; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
Pendred syndrome homolog
, sodium-independent chloride/iodide transporter
, solute carrier family 26, member 4
, Pendred's syndrome