Results 1 -
6
of
6
for
Complete congenital stationary night blindness
- ... signs and symptoms of the condition. Autosomal recessive complete congenital stationary night blindness Autosomal recessive incomplete congenital stationary night blindness Genetic ...
- ... 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; ...
- ... 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 ...
- ... 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 ...
- ... A deficiency (rare) Nontreatable causes: Birth defects, particularly congenital stationary night blindness Retinitis pigmentosa
- Cerebral Palsy (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) ...