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417 Possible Causes for X-Linked Congenital Stationary Night Blindness

  • 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] X-linked congenital stationary night blindness is almost always associated with myopia.[ncbi.nlm.nih.gov] Abstract X-linked congenital stationary night blindness (CSNB) is a nonprogressive retinal disorder characterized by disturbed or absent night vision; its clinical features[ncbi.nlm.nih.gov]

  • Occult Macular Dystrophy

    Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet. 1998;62:865–75. CrossRef PubMedCentral PubMed 8.[springermedizin.de] An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:260–3. CrossRef PubMed Google Scholar 10.[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]

  • Night Blindness

    On the other hand, the mutation of a calcium-channel gene in Xp11.23 was recently reported in incomplete X-linked congenital stationary night blindness (CSNB).[ncbi.nlm.nih.gov] Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet. 1998 Apr;62(4):865-75.[disorders.eyes.arizona.edu] Congenital Stationary Night Blindness Type 2B Congenital Stationary Night Blindness X-Linked Complete CSNB X-linked congenital stationary night blindness X-Linked Csnb X-Linked[lsd-project.jp]

  • Benign Adult Familial Myoclonic Epilepsy

    On the other hand, the mutation of a calcium-channel gene in Xp11.23 was recently reported in incomplete X-linked congenital stationary night blindness (CSNB).[ncbi.nlm.nih.gov]

  • Hyperopia

    X-linked congenital stationary night blindness is almost always associated with myopia.[ncbi.nlm.nih.gov]

  • Deafness, Autosomal Dominant 23

    1 0 Congenital stationary night blindness, autosomal dominant 1 1 Congenital stationary night blindness, autosomal recessive 10 10 Congenital stationary night blindness,[sph.uth.edu] congenital stationary night blindness X-linked dystonia-parkinsonism/Lubag Schindler disease type 1 FG syndrome 2 Absence of fingerprints congenital milia 8p23.1 duplication[checkrare.com] GNAT1, GNB3, GPR179, GRK1, GRM6, LRIT3, RDH5, SAG, SLC24A1, TRPM1 Congenital stationary night blindness, X-linked none CACNA1F, NYX Deafness alone or syndromic, autosomal[sph.uth.edu]

  • Autosomal Recessive Deafness 42

    1 0 Congenital stationary night blindness, autosomal dominant 1 1 Congenital stationary night blindness, autosomal recessive 10 10 Congenital stationary night blindness,[sph.uth.edu] GNAT1, GNB3, GPR179, GRK1, GRM6, LRIT3, RDH5, SAG, SLC24A1, TRPM1 Congenital stationary night blindness, X-linked none CACNA1F, NYX Deafness alone or syndromic, autosomal[sph.uth.edu] COD2 CACNA1F, RPGR Congenital stationary night blindness, autosomal dominant none GNAT1, PDE6B, RHO Congenital stationary night blindness, autosomal recessive none CABP4,[sph.uth.edu]

  • Non-Syndromic Ocular Stickler Syndrome Type 1 

    Diseases With Selective Loss of b Wave Amplitude on ERG Testing X-linked juvenile retinoschisis Congenital stationary night blindness Oguchi’s disease Myotonic dystrophy Batten[medtextfree.wordpress.com] Congenital Stationary Night Blindness Congenital stationary night blindness exhibits three modes of inheritance: (a) X-linked (most common), (b) autosomal dominant, and (c[entokey.com] […] recessive Oguchi’s disease, a form of congenital stationary night blindness, this phenomenon also occurs in patients who have an X-linked cone dystrophy.[15] DIAGNOSIS AND[medtextfree.wordpress.com]

  • Autosomal Recessive Deafness 24

    1 0 Congenital stationary night blindness, autosomal dominant 1 1 Congenital stationary night blindness, autosomal recessive 10 10 Congenital stationary night blindness,[sph.uth.edu] GNAT1, GNB3, GPR179, GRK1, GRM6, LRIT3, RDH5, SAG, SLC24A1, TRPM1 Congenital stationary night blindness, X-linked none CACNA1F, NYX Deafness alone or syndromic, autosomal[sph.uth.edu] COD2 CACNA1F, RPGR Congenital stationary night blindness, autosomal dominant none GNAT1, PDE6B, RHO Congenital stationary night blindness, autosomal recessive none CABP4,[sph.uth.edu]

  • Duchenne Muscular Dystrophy

    Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation: reappraisal of assignment of X linked incomplete congenital stationary night blindness[ncbi.nlm.nih.gov]

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