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701 Possible Causes for Congenital 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]

  • Familial Benign Flecked Retina

    Nystagmus, X-linked Congenital Stationary Night Blindness, Autosomal Dominant Congenital Stationary Night Blindness, Autosomal Recessive Congenital Stationary Night Blindness[oftalmic.ru] Fundus Albipunctatus (subtype) Form of congenital stationary night blindness in which patients are night-blind for life.[cram.com] blindness, congenital stationar type 1B (GRM6) Night blindness, congenital stationary type 1A (NYX) Night blindness, congenital stationary type 2A (CACNA1F) Night blindness[oftalmic.ru]

  • 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] History Exam Photos Diagnosis Teaching Points Comments Stargardt disease Differential Diagnosis Fundus albipunctatus: a form of congenital stationary night blindness with[kellogg.umich.edu] Answer: Fundus albipunctatus is a form of congenital stationary night blindness and would not be expected to produce progressive visual loss.[djo.harvard.edu]

  • 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] stationary night blindness Corneal dystrophy Doyne honeycomb dystrophy Familial exudative vitreal retinopathy Glaucoma (juvenile open-angle and congenital types only) Juvenile[columbiaeye.org]

  • Autosomal Dominant Congenital Stationary Night Blindness Type 2

    Most heterozygous (carrier) females in families with X-linked congenital stationary night blindness are asymptomatic.[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 Type 2

    Oguchi disease type 2 is a rare autosomal recessive form of congenital stationary night blindness.[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] From Wikidata Jump to navigation Jump to search human disease Oguchi disease-1 CSNBO1 congenital stationary night blindness Oguchi type 1 Night Blindness, Congenital Stationary[wikidata.org]

  • Night Blindness

    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] Congenital stationary night blindness (CSNB) refers to a group of nonprogressive retinal disorders characterized predominantly by abnormal function of the rod system.[aao.org]

  • Retinitis Pigmentosa 23

    stationary night blindness, autosomal dominant 1 1 Congenital stationary night blindness, autosomal recessive 10 10 Congenital stationary night blindness, X-linked 2 2 Leber[sph.uth.edu] […] nystagmus Myo7a congenital stationary night blindness Abca4 , Pde6b , Rbp3 , Rho , Rpgr , Sag congenital stationary night blindness autosomal dominant 1 Rho congenital stationary[rgd.mcw.edu] […] nystagmus Myo7a congenital stationary night blindness Abca4, Pde6b, Rbp3, Rho, Rpgr, Sag congenital stationary night blindness autosomal dominant 1 Rho congenital stationary[rgd.mcw.edu]

  • Retinal Pigmentary Dystrophy

    GPR125 recessive retinitis pigmentosa GPR179 Night blindness, congenital stationary GRK1 Oguchi disease GRM6 Night blindness, congenital stationary GRN Neuronal Ceroid Lipofuscinoses[molecularvisionlab.com] Stationary night blindness disorders may be classified as congenital stationary night blindness (CSNB), fundus albipunctatus, Oguchi disease and fleck retina of Kandori.[intechopen.com] blindness, congenital stationary AD/AR 5 10 GNAT2 Achromatopsia AR 7 16 GNB3 Night blindness, congenital stationary, type 1H AR 3 6 GNPTG Mucolipidosis AR 45 46 GPR179 Night[blueprintgenetics.com]

  • Sorsby Syndrome

    Stationary Night Blindness Corneal Dystrophy-Stromal Enhance S-Cone Syndrome Juvenile Open Angle Glaucoma Juvenile X-Linked Retinoschisis Leber Congenital Amaurosis Leber[medicine.uiowa.edu] GPR125 recessive retinitis pigmentosa GPR179 Night blindness, congenital stationary GRK1 Oguchi disease GRM6 Night blindness, congenital stationary GRN Neuronal Ceroid Lipofuscinoses[molecularvisionlab.com] Most common ERG pattern in Congenital Stationary Night Blindness Large A-wave and absent/small B-wave What is the defect in Congenital Stationary Night Blindness (CSNB)?[quizlet.com]

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