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515 Possible Causes for Stationary Night Blindness

  • Spasmus Nutans

    Two children with congenital stationary night blindness were originally diagnosed as having spasmus nutans.[ncbi.nlm.nih.gov] Eye and head movement recordings of patients with congenital stationary night blindness can mimic spasmus nutans.[ncbi.nlm.nih.gov] CONCLUSION: As described in patients with other retinal diseases such as achromatopsia and congenital stationary night blindness, nystagmus of patients with Bardet-Biedl syndrome[ncbi.nlm.nih.gov]

  • Congenital Stationary Night Blindness

    RESULTS: The results of ophthalmic examinations were suggestive of early-onset stationary night blindness with no extraocular anomalies.[ncbi.nlm.nih.gov] Two siblings with autosomal-recessive congenital stationary night blindness were clinically blind in infancy.[ncbi.nlm.nih.gov] Congenital stationary night blindness 2 was primarily caused by mutations in CACNA1F (55 patients, 37 families).[ncbi.nlm.nih.gov]

  • Oguchi Disease

    PURPOSE: To compare the clinical findings of the various forms of stationary night blindness caused by mutations in identified genes encoding proteins of photoreceptors or[ncbi.nlm.nih.gov] PURPOSE: To examine retinal structure and changes in photoreceptor intensity after dark adaptation in patients with complete congenital stationary night blindness and Oguchi[ncbi.nlm.nih.gov] Carroll, J ; view all (2012) Assessing retinal structure in complete congenital stationary night blindness and oguchi disease.[discovery.ucl.ac.uk]

  • Night Blindness

    Abstract In 1909, 2 years after the famous publication by Nettleship, a large family with congenital stationary night-blindness of the 'Nougaret type' was published by the[ncbi.nlm.nih.gov] Homepage Rare diseases Search Search for a rare disease Congenital stationary night blindness Disease definition Congenital stationary night blindness (CSNB) refers to a non-progressive[orpha.net] PURPOSE: To investigate photoreceptor and postreceptor retinal function in patients with congenital stationary night blindness (CSNB).[ncbi.nlm.nih.gov]

  • Fleck Retina of Kandori

    Congenital stationary night blindness SOURCES: UMLS DOID MONDO OMIM More info about OGUCHI DISEASE 2 Low match NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A NIGHT[mendelian.co] They frequently manifest as mild and stationary night blindness.[orpha.net] History Exam Photos Diagnosis Teaching Points Comments Stargardt disease Differential Diagnosis Fundus albipunctatus: a form of congenital stationary night blindness with[kellogg.umich.edu]

  • X-linked Intellectual Disability-Retinitis Pigmentosa Syndrome

    In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] Linkage analysis in X-linked congenital stationary night blindness. Genomics. 1992 Sep; 14 (1):99–104. [ PubMed ] [ Google Scholar ] Aldred MA, Wright AF.[ncbi.nlm.nih.gov] This gene codes for the rods and mutations may lead to autosomal dominant RP, autosomal dominant congenital stationary night blindness, or, rarely, autosomal recessive RP.[news-medical.net]

  • Retinitis Pigmentosa 23

    In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] night blindness, autosomal dominant 1 1 Congenital stationary night blindness, autosomal recessive 10 10 Congenital stationary night blindness, X-linked 2 2 Leber congenital[sph.uth.edu] For example, mutations of the rhodopsin gene can produce congenital stationary night blindness (CSNB), autosomal dominant RP (adRP), or autosomal recessive RP (arRP).[oxfordmedicine.com]

  • Occult Macular Dystrophy

    Establishment of the concept of new clinical entities—complete and incomplete form of congenital stationary night blindness.[springermedizin.de] Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol. 1986;104:1013–20. CrossRef PubMed Google Scholar 5.[link.springer.com] night blindness Corneal dystrophy Doyne honeycomb dystrophy Familial exudative vitreal retinopathy Glaucoma (juvenile open-angle and congenital types only) Juvenile X-linked[columbiaeye.org]

  • Bradyopsia

    Disease Type of connection Early infantile epileptic encephalopathy Congenital stationary night blindness Central areolar choroidal dystrophy Cone rod dystrophy Leber congenital[csbg.cnb.csic.es] Rarely, characteristic findings in ERG as in congenital stationary night blindness may help in arriving at a more accurate diagnosis.[egl-eurofins.com] Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness Nature Genetics 4: 280 - 283 (1993) Hamel, C.[openwetware.org]

  • Ataxia - Hypogonadism - Choroidal Dystrophy Syndrome

    In young patients with the symptom of night blindness, it is important to differentiate retinitis pigmentosa from stationary night blindness.[ommbid.mhmedical.com] night blindness, see autosomal recessive congenital stationary night blindness autosomal recessive congenital methemoglobinemia autosomal recessive congenital stationary[mygenomics.com] night blindness CACNA1F CABP4 GNAT1 GPR179 GRK1 GRM6 LRIT3 NYX PDE6B RHO SAG SLC24A1 TRPM1 Color blindness CNGA3 CNGB3 GNAT2 OPN1LW OPN1MW OPN1SW PDE6C PDE6H Usher syndrome[iovs.arvojournals.org]

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