iodine has been researched along with Hearing Loss, Sensorineural in 15 studies
Iodine: A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
diiodine : Molecule comprising two covalently bonded iodine atoms with overall zero charge..
Hearing Loss, Sensorineural: Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Slc26a4 (-/-) and (+/+) mice were fed up to 6 months on a standard or low iodine diet and were evaluated for thyroid structural abnormalities or biochemical hypothyroidism." | 7.77 | Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet. ( Bonomi, M; Bottà, G; Calebiro, D; De Nittis, D; Fugazzola, L; Grindati, A; Lisi, S; Marinò, M; Persani, L; Porazzi, P, 2011) |
| "Pendred Syndrome, first described in 1896, is phenotypically characterized as the coexistence of sensorineural deafness and enlarged goiter with elevated iodine discharge after perchlorate administration." | 4.82 | Pendred syndrome. ( Glaser, B, 2003) |
| "Slc26a4 (-/-) and (+/+) mice were fed up to 6 months on a standard or low iodine diet and were evaluated for thyroid structural abnormalities or biochemical hypothyroidism." | 3.77 | Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet. ( Bonomi, M; Bottà, G; Calebiro, D; De Nittis, D; Fugazzola, L; Grindati, A; Lisi, S; Marinò, M; Persani, L; Porazzi, P, 2011) |
| "Pendred syndrome (PS) is an autosomal recessive disease that is characterized by congenital sensorineural hearing loss, goiter, and a partial iodine organification defect." | 3.74 | Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan. ( Chiu, CY; Jap, TS; Lai, CC; Shiao, AS; Tso, YC; Tu, TY; Wu, YC, 2007) |
| "Pendred syndrome is an autosomal recessive inherited disorder characterized by profound hearing impairment and inappropriate iodine release by the thyroid on perchlorate challenge." | 3.72 | Neuro-otological findings in Pendred syndrome. ( Britton, KE; Coffey, RA; Cohen, M; Jan, H; Luxon, LM; Phelps, PD; Reardon, W; Trembath, RC, 2003) |
| "Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/hearing impairment, goiter, and an abnormal organification of iodide with or without hypothyroidism." | 2.55 | Pendred syndrome. ( Kopp, P; Wémeau, JL, 2017) |
| "Pendred syndrome is often associated with inner ear malformations, especially enlarged vestibular aqueduct (EVA)." | 1.31 | Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene. ( Furuhashi, A; Miura, Y; Mori, N; Murakami, H; Naganawa, S; Nakashima, T; Nakayama, A; Sato, E; Tadokoro, M, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (13.33) | 18.7374 |
| 1990's | 1 (6.67) | 18.2507 |
| 2000's | 10 (66.67) | 29.6817 |
| 2010's | 2 (13.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wémeau, JL | 1 |
| Kopp, P | 2 |
| Calebiro, D | 1 |
| Porazzi, P | 1 |
| Bonomi, M | 1 |
| Lisi, S | 1 |
| Grindati, A | 1 |
| De Nittis, D | 1 |
| Fugazzola, L | 1 |
| Marinò, M | 1 |
| Bottà, G | 1 |
| Persani, L | 1 |
| Luxon, LM | 1 |
| Cohen, M | 1 |
| Coffey, RA | 1 |
| Phelps, PD | 1 |
| Britton, KE | 1 |
| Jan, H | 1 |
| Trembath, RC | 1 |
| Reardon, W | 1 |
| HENI, F | 1 |
| SIEBNER, H | 1 |
| Bogazzi, F | 1 |
| Russo, D | 1 |
| Raggi, F | 1 |
| Ultimieri, F | 1 |
| Berrettini, S | 1 |
| Forli, F | 1 |
| Grasso, L | 1 |
| Ceccarelli, C | 1 |
| Mariotti, S | 1 |
| Pinchera, A | 1 |
| Bartalena, L | 1 |
| Martino, E | 1 |
| Hiyoshi, M | 1 |
| Yamane, H | 1 |
| Glaser, B | 1 |
| Lai, CC | 1 |
| Chiu, CY | 1 |
| Shiao, AS | 1 |
| Tso, YC | 1 |
| Wu, YC | 1 |
| Tu, TY | 1 |
| Jap, TS | 1 |
| Palos, F | 1 |
| García-Rendueles, ME | 1 |
| Araujo-Vilar, D | 1 |
| Obregon, MJ | 1 |
| Calvo, RM | 1 |
| Cameselle-Teijeiro, J | 1 |
| Bravo, SB | 1 |
| Perez-Guerra, O | 1 |
| Loidi, L | 1 |
| Czarnocka, B | 1 |
| Alvarez, P | 1 |
| Refetoff, S | 1 |
| Dominguez-Gerpe, L | 1 |
| Alvarez, CV | 1 |
| Lado-Abeal, J | 1 |
| Scott, DA | 1 |
| Wang, R | 1 |
| Kreman, TM | 1 |
| Andrews, M | 1 |
| McDonald, JM | 1 |
| Bishop, JR | 1 |
| Smith, RJ | 1 |
| Karniski, LP | 1 |
| Sheffield, VC | 1 |
| Bidart, JM | 1 |
| Lacroix, L | 1 |
| Evain-Brion, D | 1 |
| Caillou, B | 1 |
| Lazar, V | 1 |
| Frydman, R | 1 |
| Bellet, D | 1 |
| Filetti, S | 1 |
| Schlumberger, M | 1 |
| Gao, H | 1 |
| Li, J | 1 |
| Wang, E | 1 |
| Gonzalez Trevino, O | 1 |
| Karamanoglu Arseven, O | 1 |
| Ceballos, CJ | 1 |
| Vives, VI | 1 |
| Ramirez, RC | 1 |
| Gomez, VV | 1 |
| Medeiros-Neto, G | 1 |
| Sato, E | 1 |
| Nakashima, T | 1 |
| Miura, Y | 1 |
| Furuhashi, A | 1 |
| Nakayama, A | 1 |
| Mori, N | 1 |
| Murakami, H | 1 |
| Naganawa, S | 1 |
| Tadokoro, M | 1 |
| Boyages, SC | 1 |
| Collins, JK | 1 |
| Maberly, GF | 1 |
| Jupp, JJ | 1 |
| Morris, J | 1 |
| Eastman, CJ | 1 |
2 reviews available for iodine and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Pendred syndrome.
Topics: Anoctamin-1; Goiter, Nodular; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Iodides; Iodine; | 2017 |
Pendred syndrome.
Topics: Biological Transport; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membrane Transport Protei | 2003 |
13 other studies available for iodine and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.
Topics: Animals; Anion Transport Proteins; Diet; Disease Models, Animal; Goiter; Goiter, Nodular; Hearing Lo | 2011 |
Neuro-otological findings in Pendred syndrome.
Topics: Adolescent; Adult; Audiometry, Pure-Tone; Child; Ear, Inner; Female; Hearing Loss, Sensorineural; Hu | 2003 |
[STRUCTURAL AND NUMERICAL CHROMOSOME PATTERN (GROUP A AND E) IN A GIRL WITH THE PENDRED SYNDROME].
Topics: Adolescent; Cell Division; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Dwarfism; Fema | 1963 |
Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.
Topics: Adolescent; Adult; Audiometry; Child; DNA; Female; Goiter; Hearing Loss, Sensorineural; Humans; Iodi | 2004 |
A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss.
Topics: Consanguinity; Female; Genes, Recessive; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membra | 2004 |
Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
Topics: Abnormalities, Multiple; Adolescent; Adult; Base Sequence; Case-Control Studies; Child; DNA Mutation | 2007 |
Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.
Topics: Adult; Amino Acid Sequence; Female; Goiter, Nodular; Haplotypes; Hearing Loss, Sensorineural; Humans | 2008 |
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).
Topics: Alleles; Amino Acid Substitution; Animals; Carrier Proteins; Female; Genetic Variation; Goiter; Hear | 2000 |
Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells.
Topics: Carrier Proteins; Cells, Cultured; Chorionic Gonadotropin; Female; Goiter; Hearing Loss, Bilateral; | 2000 |
[Iodine deficiency and perceptive nerve deafness].
Topics: Adolescent; Child; Child, Preschool; Female; Hair; Hearing Loss, Sensorineural; Humans; Iodine; Male | 1998 |
Clinical and molecular analysis of three Mexican families with Pendred's syndrome.
Topics: Adolescent; Child; Female; Goiter; Haplotypes; Hearing Loss, Sensorineural; Humans; Iodides; Iodine; | 2001 |
Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene.
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Carrier Proteins; Child; Endolymphati | 2001 |
Iodine deficiency impairs intellectual and neuromotor development in apparently-normal persons. A study of rural inhabitants of north-central China.
Topics: Adolescent; Adult; Audiometry; Child; China; Cognition Disorders; Cohort Studies; Congenital Hypothy | 1989 |