Results 1 -
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369
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Vision disorder
- ... GNAT2 gene have been found to cause the vision disorder achromatopsia. These mutations are a relatively uncommon cause ... with incomplete achromatopsia, a milder form of the disorder associated with limited color vision.The GNAT2 gene mutations that underlie complete achromatopsia ...
- ... CNGA3 gene have been found to cause the vision disorder achromatopsia. These mutations underlie about 25 percent of ... with incomplete achromatopsia, a milder form of the disorder associated with limited color vision.The CNGA3 gene mutations that underlie complete achromatopsia ...
- ... PDE6C gene have been found to cause the vision disorder achromatopsia. These mutations underlie a relatively small percentage ... with incomplete achromatopsia, a milder form of the disorder associated with limited color vision.The PDE6C gene mutations associated with achromatopsia affect ...
- ... CNGB3 gene have been found to cause the vision disorder achromatopsia. These mutations cause 50 to 70 percent ... cases of complete achromatopsia, a form of the disorder characterized by a total lack of color vision and other vision problems that are present from ...
- ... have been reported to cause retinitis pigmentosa, a vision disorder that causes the light-sensing cells of the ... characterized by a combination of hearing loss and vision loss associated with ... a form of the disorder known as Usher syndrome type IIA (USH2A), which ...
- ... children thought to have DFNB12 have developed the vision disorder retinitis pigmentosa later in life, which is characteristic ... is characterized by a combination of hearing loss, vision loss, and ... cause a form of the disorder known as Usher syndrome type ID (USH1D).Most ...
- ... have nonsyndromic hearing loss developed retinitis pigmentosa (a vision disorder characteristic of Usher syndrome) later in life. However, ... is characterized by a combination of hearing loss, vision loss, and problems ... a form of the disorder known as Usher syndrome type IB (USH1B), which ...
- ... PDE6H gene has been found to cause the vision disorder achromatopsia. It is a very rare cause of a form of the disorder called incomplete achromatopsia. This condition is characterized by limited color vision and other vision problems that are present from ...
- ... gene have been identified in people with a vision disorder called cone-rod dystrophy. The problems associated with ... loss of these cells leads to the progressive vision problems characteristic of cone-rod ... condition is an eye disorder that primarily affects the retina. People with this ...
- ... ABCA4 gene have been found to cause a vision disorder called cone-rod dystrophy. The problems associated with ... to light (photophobia), and impaired color vision. These vision problems ... a variant to cause the disorder.Most of the ABCA4 gene variants that cause ...
