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Results 1 - 6 of 6 for Complete congenital stationary night blindness
  1. ... signs and symptoms of the condition. Autosomal recessive complete congenital stationary night blindness Autosomal recessive incomplete congenital stationary night blindness Genetic ...
  2. ... TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ... TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. Am J Hum Genet. 2009 Nov; ...
  3. ... the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nat Genet. 2000 Nov;26(3):319-23. ... Sylla E, Pusch CM. Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX ...
  4. ... the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nat Genet. 2000 Nov;26(3):319-23. ... Sylla E, Pusch CM. Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX ...
  5. ... A deficiency (rare) Nontreatable causes: Birth defects, particularly congenital stationary night blindness Retinitis pigmentosa
  6. Cerebral Palsy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebral Palsy/Start Here ... Cerebral Palsy ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Cerebral palsy (CP) ...