Matches in SemOpenAlex for { <https://semopenalex.org/work/W139804938> ?p ?o ?g. }
Showing items 1 to 100 of
100
with 100 items per page.
- W139804938 endingPage "242" @default.
- W139804938 startingPage "238" @default.
- W139804938 abstract "Norrie disease (ND) is a rare X-linked recessive disorder characterized by congenital blindness, which is often associated with sensorineural hearing loss and mental retardation. X-linked familial exudative vitreoretinopathy (FEVR) is a hereditary disorder characterized by an abnormality of the peripheral retina and is not associated with systemic diseases. X-linked recessive disorders generally do not affect females. Here we show that female carriers can be associated with manifestation of an X-linked disorder.A four-generation family with an affected female, and a history of congenital blindness and hearing loss, was identified through the pro-band. A second family, with a full-term female infant, was evaluated through ophthalmic examinations and found to exhibit ocular features, such as retinal folds, retinal detachment and peripheral exudates. Peripheral blood specimens were collected from several affected and unaffected family members. DNA was extracted and analyzed by single-strand conformation polymorphism (SSCP) following polymerase chain reaction (PCR) amplification of the exons of the Norrie disease gene. The amplified products were sequenced by the dideoxy chain termination method.In an X-linked four-generation family, a novel missense (A118D) mutation in the third exon of the Norrie disease gene, was identified. The mutation was transmitted through three generations and cosegregated with the disease. The affected maternal grandmother and the unaffected mother carried the same mutation in one of their alleles. In an unrelated sporadic family, a heterozygous missense mutation (C96Y) was identified in the third exon of the Norrie disease gene in an affected individual. Analysis of exon-1 and 2 of the Norrie disease gene did not reveal any additional sequence alterations in these families. The mutations were not detected in the unaffected family members and the 116 normal unrelated controls, suggesting that they are likely to be the pathogenic mutations.The results further strengthen the proposal that X-linked disorders can occur in female carriers, due likely to an unfavorable X-inactivation." @default.
- W139804938 created "2016-06-24" @default.
- W139804938 creator A5029908022 @default.
- W139804938 creator A5039096233 @default.
- W139804938 creator A5049049244 @default.
- W139804938 creator A5083609672 @default.
- W139804938 date "1999-07-01" @default.
- W139804938 modified "2023-09-23" @default.
- W139804938 title "Norrie Disease and Exudative Vitreoretinopathy in Families with Affected Female Carriers" @default.
- W139804938 cites W1501879711 @default.
- W139804938 cites W1520169630 @default.
- W139804938 cites W1985106697 @default.
- W139804938 cites W2003915580 @default.
- W139804938 cites W2005346444 @default.
- W139804938 cites W2012618832 @default.
- W139804938 cites W2020757970 @default.
- W139804938 cites W2021278461 @default.
- W139804938 cites W2034961254 @default.
- W139804938 cites W2039980802 @default.
- W139804938 cites W2040041683 @default.
- W139804938 cites W2040995502 @default.
- W139804938 cites W2044322648 @default.
- W139804938 cites W2044727165 @default.
- W139804938 cites W2046194964 @default.
- W139804938 cites W2052742602 @default.
- W139804938 cites W2057175927 @default.
- W139804938 cites W2069325164 @default.
- W139804938 cites W2070948073 @default.
- W139804938 cites W2078458577 @default.
- W139804938 cites W2087188447 @default.
- W139804938 cites W2323110199 @default.
- W139804938 cites W2562585785 @default.
- W139804938 doi "https://doi.org/10.1177/112067219900900312" @default.
- W139804938 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10544980" @default.
- W139804938 hasPublicationYear "1999" @default.
- W139804938 type Work @default.
- W139804938 sameAs 139804938 @default.
- W139804938 citedByCount "27" @default.
- W139804938 countsByYear W1398049382012 @default.
- W139804938 countsByYear W1398049382013 @default.
- W139804938 countsByYear W1398049382016 @default.
- W139804938 countsByYear W1398049382018 @default.
- W139804938 countsByYear W1398049382019 @default.
- W139804938 countsByYear W1398049382021 @default.
- W139804938 countsByYear W1398049382022 @default.
- W139804938 crossrefType "journal-article" @default.
- W139804938 hasAuthorship W139804938A5029908022 @default.
- W139804938 hasAuthorship W139804938A5039096233 @default.
- W139804938 hasAuthorship W139804938A5049049244 @default.
- W139804938 hasAuthorship W139804938A5083609672 @default.
- W139804938 hasConcept C104317684 @default.
- W139804938 hasConcept C118487528 @default.
- W139804938 hasConcept C180754005 @default.
- W139804938 hasConcept C2780428090 @default.
- W139804938 hasConcept C2780493683 @default.
- W139804938 hasConcept C2780827179 @default.
- W139804938 hasConcept C2910227669 @default.
- W139804938 hasConcept C36823959 @default.
- W139804938 hasConcept C501734568 @default.
- W139804938 hasConcept C54355233 @default.
- W139804938 hasConcept C548259974 @default.
- W139804938 hasConcept C71924100 @default.
- W139804938 hasConcept C75563809 @default.
- W139804938 hasConcept C86803240 @default.
- W139804938 hasConceptScore W139804938C104317684 @default.
- W139804938 hasConceptScore W139804938C118487528 @default.
- W139804938 hasConceptScore W139804938C180754005 @default.
- W139804938 hasConceptScore W139804938C2780428090 @default.
- W139804938 hasConceptScore W139804938C2780493683 @default.
- W139804938 hasConceptScore W139804938C2780827179 @default.
- W139804938 hasConceptScore W139804938C2910227669 @default.
- W139804938 hasConceptScore W139804938C36823959 @default.
- W139804938 hasConceptScore W139804938C501734568 @default.
- W139804938 hasConceptScore W139804938C54355233 @default.
- W139804938 hasConceptScore W139804938C548259974 @default.
- W139804938 hasConceptScore W139804938C71924100 @default.
- W139804938 hasConceptScore W139804938C75563809 @default.
- W139804938 hasConceptScore W139804938C86803240 @default.
- W139804938 hasIssue "3" @default.
- W139804938 hasLocation W1398049381 @default.
- W139804938 hasLocation W1398049382 @default.
- W139804938 hasOpenAccess W139804938 @default.
- W139804938 hasPrimaryLocation W1398049381 @default.
- W139804938 hasRelatedWork W1973942562 @default.
- W139804938 hasRelatedWork W2028070898 @default.
- W139804938 hasRelatedWork W2060169551 @default.
- W139804938 hasRelatedWork W2068932327 @default.
- W139804938 hasRelatedWork W2258430434 @default.
- W139804938 hasRelatedWork W2349400098 @default.
- W139804938 hasRelatedWork W2350102540 @default.
- W139804938 hasRelatedWork W2362650105 @default.
- W139804938 hasRelatedWork W2409341427 @default.
- W139804938 hasRelatedWork W2419448289 @default.
- W139804938 hasVolume "9" @default.
- W139804938 isParatext "false" @default.
- W139804938 isRetracted "false" @default.
- W139804938 magId "139804938" @default.
- W139804938 workType "article" @default.