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non-syndromic deafness - inherited deafness not related to other malformations Definition for non-syndromic deafness http://www.genetics.org.uk/genetics_of_non-syndromic_deafness some common symptoms hearing loss some related diagnoses 1 - 7 of 100 diagnoses cerumen impaction perforated ear drum otitis media malignant external otitis herpes zoster oticus Meniere's disease ciliary dyskinesia   more do i have 'non-syndromic deafness'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'non-syndromic deafness' 1 - 5 of 6 diagnostic tests Molecular Genetic Studies non-syndromic deafness and Molecular Genetic Studies Hearing test standard technique of representing hearing loss non-syndromic deafness and Hearing test Refraction non-syndromic deafness and Refraction Brainstem auditory evoked response (BAER) non-syndromic deafness and Brainstem auditory evoked response (BAER) Comprehensive eye exam non-syndromic deafness and Comprehensive eye exam speech reception threshold (SRT) non-syndromic deafness and speech reception threshold (SRT) for more please login, login is free (click to login) therapeutic procedures for 'non-syndromic deafness'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for non-syndromic deafness: therapeutic procedure search results for 'non-syndromic deafness' 1 - 2 of 2 therapeutic procedures rankings are computer generated. please consult your health care provider. Cochlear implants non-syndromic deafness and Cochlear implants Speech Therapy non-syndromic deafness and Speech Therapy medications search results for 'non-syndromic deafness' 1 - 2 of 2 medications rankings are computer generated. please consult your health care provider.   Acetaminophen non-syndromic deafness and Acetaminophen   streptomycin non-syndromic deafness and streptomycin web search results for non-syndromic deafness Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - non-syndromic deafness Phenotype of non-syndromic deafness associated with the mitochondrial ... Phenotype of non-syndromic deafness associated with the mitochondrial A1555G ... or rRNA modification, and two genes associated with non-syndromic deafness, for ... http://www.ncbi.nlm.nih.gov/pubmed/15542390   www.ncbi.nlm.nih.gov - summary Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness ... ... of DFN3 non-syndromic deafness: morphologic and immunohistochemical ... males and females of a mouse model of DFN3 non-syndromic deafness generated by ... http://www.ncbi.nlm.nih.gov/pubmed/12062767   www.ncbi.nlm.nih.gov - summary A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps ... A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13 ... Non-syndromic hearing loss is the most common sensory disorder in humans; 15%-20 ... http://www.ncbi.nlm.nih.gov/pubmed/12596055   www.ncbi.nlm.nih.gov - summary Autosomal dominant non-syndromic deafness caused by a mutation in the ... Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. ... Support, Non-U.S. Gov't. Mesh Terms: Deafness/genetics* Genes, ... http://www.ncbi.nlm.nih.gov/pubmed/9354784   www.ncbi.nlm.nih.gov - summary Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Over 25 loci involved in non-syndromic deafness have been mapped and mutations ... By screening families with non-syndromic deafness from China, we have identified ... http://www.ncbi.nlm.nih.gov/pubmed/9171832   www.ncbi.nlm.nih.gov - summary Genomics|HuGENet|Reviews|References|GJB2 and hearing loss|PubMed ID ... Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. ... mutation in the connexin 26 gene associated with dominant non-syndromic deafness. ... http://www.cdc.gov/genomics/hugenet/reviews/tables/GJB2_Ref.htm   www.cdc.gov - summary Non-syndromic, autosomal-recessive deafness. Non-syndromic, autosomal-recessive deafness. Petersen MB, Willems PJ. ... Non-syndromic deafness is a paradigm of genetic heterogeneity with 85 loci and ... http://www.ncbi.nlm.nih.gov/pubmed/16650073?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary STRC - References - Genetics Home Reference Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. Review. ... of the hair bundle cause non-syndromic deafness at the DFNB16 locus. ... http://ghr.nlm.nih.gov/gene=strc/show/References   ghr.nlm.nih.gov - summary Nonsyndromic deafness - Wikipedia, the free encyclopedia In contrast, syndromic deafness involves hearing loss that occurs with ... late-onset deafness is autosomal dominant and non-syndromic (Van Camp et al., 1997) ... http://en.wikipedia.org/wiki/Nonsyndromic_deafness   en.wikipedia.org - summary Genomics|Training|Books|HuGE|Part 4, Chapter 24 Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997;387:80-83. ... mutations in autosomal recessive non-syndromic deafness. ... http://www.cdc.gov/genomics/training/books/HuGE/chap24.htm   www.cdc.gov - summary SLC26A4 - References - Genetics Home Reference A mutation in PDS causes non-syndromic recessive deafness. Nat Genet. ... The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4. Adv Otorhinolaryngol. ... http://ghr.nlm.nih.gov/gene=slc26a4/show/References   ghr.nlm.nih.gov - summary USH1C - References - Genetics Home Reference ... mutations to syndromic and non-syndromic deafness in the UK. ... the alternatively spliced exons of USH1C cause non-syndromic recessive deafness. Hum Genet. ... http://ghr.nlm.nih.gov/gene=ush1c/show/References   ghr.nlm.nih.gov - summary A mutation in PDS causes non-syndromic recessive deafness. ... Genet. 1998 Mar;18(3):215-7. A mutation in PDS causes non-syndromic recessive deafness. Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ... http://www.ncbi.nlm.nih.gov/pubmed/9500541   www.ncbi.nlm.nih.gov - summary A gene for a dominant form of non-syndromic sensorineural deafness ... ... a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the ... that another gene for dominant non-syndromic hearing loss (DFNA3) has been ... http://www.ncbi.nlm.nih.gov/pubmed/8776602   www.ncbi.nlm.nih.gov - summary Nonsyndromic deafness - References - Genetics Home Reference Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. Review. ... Non-syndromic autosomal-dominant deafness. Clin Genet. 2002 Jul;62 ... http://ghr.nlm.nih.gov/condition=nonsyndromicdeafness/show/References   ghr.nlm.nih.gov - summary Mutations in the alternatively spliced exons of USH1C cause non ... Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness. ... a form of non-syndromic deafness, which maps to a chromosomal ... http://www.ncbi.nlm.nih.gov/pubmed/12136232   www.ncbi.nlm.nih.gov - summary Pendred syndrome - References - Genetics Home Reference ... Pendred syndrome and non-syndromic EVA are distinct clinical ... The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4. Adv Otorhinolaryngol. ... http://ghr.nlm.nih.gov/condition=pendredsyndrome/show/Sources+for+this+page   ghr.nlm.nih.gov - summary Hereditary deafness and phenotyping in humans. ... be undertaken in all cases of non-syndromic deafness where the cause cannot be ... Most forms of non-syndromic autosomal recessive hearing impairment cause a ... http://www.ncbi.nlm.nih.gov/pubmed/12324385   www.ncbi.nlm.nih.gov - summary Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 ... ... while in other families the deafness is non-syndromic and there is no other ... Eastern Druze family with recessive non-syndromic deafness and demonstrate ... http://www.ncbi.nlm.nih.gov/pubmed/8541853   www.ncbi.nlm.nih.gov - summary Mutations in connexin31 underlie recessive as well as dominant non ... ... can also cause recessive non-syndromic deafness, we screened 25 Chinese families ... lead to both recessive and dominant forms of non-syndromic deafness. ... http://www.ncbi.nlm.nih.gov/pubmed/10587579   www.ncbi.nlm.nih.gov - summary Mutations in GJA1 (connexin 43) are associated with non-syndromic ... Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness. ... connexin gene to be associated with non-syndromic deafness. ... http://www.ncbi.nlm.nih.gov/pubmed/11741837?dopt=Abstract   www.ncbi.nlm.nih.gov - summary A novel TECTA mutation confirms the recognizable phenotype among ... The TECTA autosomal recessive non-syndromic deafness phenotype differs from the ... is seen in most families segregating autosomal recessive non-syndromic deafness. ... http://www.ncbi.nlm.nih.gov/pubmed/18022253?ordinalpos=2&ito...   www.ncbi.nlm.nih.gov - summary Mitochondrial ribosomal RNA mutation associated with both antibiotic ... ... RNA mutation associated with both antibiotic-induced and non-syndromic deafness. ... Maternally transmitted non-syndromic deafness was described recently both in ... http://www.ncbi.nlm.nih.gov/pubmed/7689389   www.ncbi.nlm.nih.gov - summary Mutations in a new gene encoding a protein of the hair bundle cause non ... ... a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus. ... 70 loci implicated in non-syndromic forms of deafness have been reported in ... http://www.ncbi.nlm.nih.gov/pubmed/11687802   www.ncbi.nlm.nih.gov - summary Mutations of human TMHS cause recessively inherited non-syndromic ... RESULTS: A novel locus for non-syndromic deafness DFNB67 was mapped in an ... of two families segregating non-syndromic deafness, one of which showed ... http://www.ncbi.nlm.nih.gov/pubmed/16459341   www.ncbi.nlm.nih.gov - summary CLDN14 - References - Genetics Home Reference ... model for autosomal recessive deafness DFNB29, are deaf due to ... Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. Review. ... http://ghr.nlm.nih.gov/gene=cldn14/show/References   ghr.nlm.nih.gov - summary Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 ... Non-syndromic deafness is genetically heterogeneous. ... syndromic recessive deafness at the DFNB7/B11 locus on chromosome 9q13-q21 in ... http://www.ncbi.nlm.nih.gov/pubmed/17877751   www.ncbi.nlm.nih.gov - summary General Hearing Loss, FAQs, EHDI, NCBDDD, CDC Hearing, Ear, Infections, and Deafness. ... No, infants with hearing loss have either a non-syndromic form or a syndromic form. ... http://www.cdc.gov/ncbddd/ehdi/FAQ/questionsgeneralHL.htm   www.cdc.gov - summary An alpha-tectorin gene defect causes a newly identified autosomal ... ... recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. ... responsible for non-syndromic autosomal recessive forms of deafness, DFNB loci, ... http://www.ncbi.nlm.nih.gov/pubmed/9949200   www.ncbi.nlm.nih.gov - summary COCH - References - Genetics Home Reference Human nonsyndromic sensorineural deafness. Annu Rev Genomics Hum Genet. ... in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of ... http://ghr.nlm.nih.gov/gene=coch/show/References   ghr.nlm.nih.gov - summary MYO7A - Wikipedia, the free encyclopedia ... form of non-syndromic sensorineural deafness (DFNA11) maps ... Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. ... http://en.wikipedia.org/wiki/MYO7A   en.wikipedia.org - summary GJB3 - References - Genetics Home Reference ... 31 (GJB3) alterations and sensorineural deafness in Austria. ... Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. Review. ... http://ghr.nlm.nih.gov/gene=gjb3/show/References   ghr.nlm.nih.gov - summary Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous ... ... deafness of Wolfram syndrome patients and lacks any syndromic ... might be a cause of non-syndromic deafness in the general population should be explored. ... http://www.ncbi.nlm.nih.gov/pubmed/11709538   www.ncbi.nlm.nih.gov - summary A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents ... ... the importance of this gene in non-syndromic childhood or congenital deafness ... a considerable contributor to non-syndromic deafness in the Turkish population. ... http://www.ncbi.nlm.nih.gov/pubmed/16021470   www.ncbi.nlm.nih.gov - summary A human gene responsible for neurosensory, non-syndromic recessive ... ... responsible for neurosensory, non-syndromic recessive deafness is a candidate ... of mouse models for the various forms of human neurosensory non-syndromic ... http://www.ncbi.nlm.nih.gov/pubmed/7951250   www.ncbi.nlm.nih.gov - summary A large deletion including most of GJB6 in recessive non syndromic ... A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect? ... of the recessive non syndromic deafness (DFNB1) among 30 ... http://www.ncbi.nlm.nih.gov/pubmed/11896458   www.ncbi.nlm.nih.gov - summary GJB2 - References - Genetics Home Reference Human nonsyndromic sensorineural deafness. Annu Rev Genomics Hum Genet. ... Non-syndromic, autosomal-recessive deafness. Clin Genet. 2006 May;69(5):371-92. Review. ... http://ghr.nlm.nih.gov/gene=gjb2/show/References   ghr.nlm.nih.gov - summary Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive ... ... to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families. ... locus (DFNB1) responsible for non-syndromic neurosensory ... http://www.ncbi.nlm.nih.gov/pubmed/9195157?dopt=Abstract   www.ncbi.nlm.nih.gov - summary TECTA - Wikipedia, the free encyclopedia ... gene cause autosomal dominant non-syndromic hearing impairment. ... recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.". Hum. ... http://en.wikipedia.org/wiki/TECTA   en.wikipedia.org - summary Nonsyndromic Hearing Loss and Deafness, DFNB1 -- GeneReviews -- NCBI ... Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature. ... in PDS causes non-syndromic recessive deafness. Nat Genet. 1998; 18: ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=dfnb1   www.ncbi.nlm.nih.gov - summary Novel missense mutations of TMPRSS3 in two consanguineous Tunisian ... ... Tunisian families with non-syndromic autosomal recessive deafness. ... for two non-syndromic recessive deafness loci located on human chromosome 21q22. ... http://www.ncbi.nlm.nih.gov/pubmed/11462234   www.ncbi.nlm.nih.gov - summary Prestin, a cochlear motor protein, is defective in non-syndromic ... Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. ... is responsible for recessive non-syndromic deafness in two unrelated families. ... http://www.ncbi.nlm.nih.gov/pubmed/12719379   www.ncbi.nlm.nih.gov - summary Mutations of ESPN cause autosomal recessive deafness and vestibular ... We mapped a human deafness locus DFNB36 to chromosome 1p36.3 in two ... marker for refining the differential diagnosis of non-syndromic deafness. Publication Types: ... http://www.ncbi.nlm.nih.gov/pubmed/15286153?dopt=Abstract   www.ncbi.nlm.nih.gov - summary A novel gene for Usher syndrome type 2: mutations in the long isoform ... ... of whirlin have previously been reported in non-syndromic ... this is the first case of USH2 that is allelic to non-syndromic deafness. Publication Types: ... http://www.ncbi.nlm.nih.gov/pubmed/17171570   www.ncbi.nlm.nih.gov - summary Mutations in the gene encoding gap junction protein beta-3 associated ... More than 50% of the cases of profound early-onset deafness are caused by genetic factors. Over 40 loci for non-syndromic deafness have been genetically mapped, and ... http://www.ncbi.nlm.nih.gov/pubmed/9843210   www.ncbi.nlm.nih.gov - summary Talk:Hearing impairment/Deafness - Wikipedia, the free encyclopedia 3.1.1 Non-syndromic. 3.1.2 Syndromic deafness. 3.2 Environmental causes ... [edit] Non-syndromic. Main article: Nonsyndromic deafness ... http://en.wikipedia.org/wiki/Talk:Hearing_impairment/Deafness   en.wikipedia.org - summary TMPRSS3, a type II transmembrane serine protease mutated in non ... ... serine protease mutated in non-syndromic autosomal recessive deafness. ... in TMPRSS3 were responsible for autosomal recessive non-syndromic hearing loss. ... http://www.ncbi.nlm.nih.gov/pubmed/17981648   www.ncbi.nlm.nih.gov - summary Prelingual deafness: high prevalence of a 30delG mutation in the ... Prelingual non-syndromic (isolated) deafness is the most frequent hereditary sensory defect. ... deafness was shown to be linked to the DFNB1 locus, 10 are small non ... http://www.ncbi.nlm.nih.gov/pubmed/9336442   www.ncbi.nlm.nih.gov - summary Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). In both families, deafness is non-progressive and predominantly affects middle frequencies. ... architecture associated with non-syndromic hearing loss, and ... http://www.ncbi.nlm.nih.gov/pubmed/10581026   www.ncbi.nlm.nih.gov - summary A biochemical basis for the inherited susceptibility to aminoglycoside ... ... to be associated with non-syndromic deafness and aminoglycoside-induced deafness. ... Deafness/genetics* Female. Genetic Predisposition to Disease. Humans ... http://www.ncbi.nlm.nih.gov/pubmed/10915767   www.ncbi.nlm.nih.gov - summary show more 1  2