postlingual

См. также в других словарях:

• postlingual — post·lin·gual liŋ g(yə )wəl adj occurring after an individual has developed the use of language <postlingual deafness> post·lin·gual·ly ē adv * * * post·lin·gual (pōst lingґgwəl) 1. occurring after the development of language. 2.… …   Medical dictionary

• postlingual fissure — fissura precentralis cerebelli …   Medical dictionary

• postlingual hearing loss — hearing loss that occurs after the person has learned to speak …   Medical dictionary

• Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… …   Wikipedia

• COCH — Coagulation factor C homolog, cochlin (Limulus polyphemus), also known as COCH, is a human gene.cite web | title = Entrez Gene: COCH coagulation factor C homolog, cochlin (Limulus polyphemus)| url =… …   Wikipedia

• TMPRSS3 — Transmembrane protease, serine 3, also known as TMPRSS3, is a human gene.cite web | title = Entrez Gene: TMPRSS3 transmembrane protease, serine 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=64699|… …   Wikipedia

• TECTA — Tectorin alpha, also known as TECTA, is a human gene.cite web | title = Entrez Gene: TECTA tectorin alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7007| accessdate = ] PBB Summary section title =… …   Wikipedia

• EYA4 — Eyes absent homolog 4 (Drosophila), also known as EYA4, is a human gene.cite web | title = Entrez Gene: EYA4 eyes absent homolog 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2070|… …   Wikipedia

• TMC1 — Transmembrane channel like 1, also known as TMC1, is a human gene.cite web | title = Entrez Gene: TMC1 transmembrane channel like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=117531| accessdate = ] PBB …   Wikipedia

• Usher-Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie H90.3 …   Deutsch Wikipedia

• Usher Syndrom — Klassifikation nach ICD 10 Q87.8 Usher Syndrom H35.5 Hereditäre Netzhautdystrophie …   Deutsch Wikipedia