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Myopia "1," "X-linked"
- ... NORD) ClinicalTrials.gov MYOPIA 2, AUTOSOMAL DOMINANT; MYP2 MYOPIA 1, X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, AUTOSOMAL RECESSIVE; ...
- ... least one other CACNA1F mutation is responsible for X-linked cone-rod ... of the alpha-1 subunit, which likely prevents the production of functional ...
- ... NYX gene have been found to cause high myopia without the other vision problems characteristic of X-linked congenital stationary night blindness. The mutations responsible for ...
- ... although it is much less common than nearsightedness (myopia) or presbyopia. The prevalence of hyperopia decreases with age: most infants are farsighted at birth, but less than 4 percent of children have the condition at age 1. The prevalence continues to decrease into adulthood. Most ...
- ... back-and-forth eye movements (nystagmus), and nearsightedness (myopia). Blue cone ... Northern European ancestry, it occurs in about 1 in 12 males and 1 in 200 females. ...
- ... the condition.Less commonly, isolated coloboma may have X-linked dominant or X-linked recessive patterns of inheritance. X-linked means that a gene associated with this condition ...
- Nystagmus (American Association for Pediatric Ophthalmology and Strabismus)Eye Movement Disorders/Start Here ... Eye Movement Disorders ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows a single glossary entry ... American ...