-
degeneration (rhodopsin mutation)
Retinitis pigmentosa GTPase regulator Retinitis Pigmentosa International "Facts
About Retinitis Pigmentosa".
National Eye Institute...
- eye's "sensing" tissue.
Retinitis may be
caused by a
number of
different infectious agents. Its most
common form,
called retinitis pigmentosa, has a prevalence...
-
Cytomegalovirus retinitis, also
known as CMV
retinitis, is an
inflammation of the
retina of the eye that can lead to blindness.
Caused by
human cytomegalovirus...
-
Usher syndrome, also
known as
Hallgren syndrome, Usher–Hallgren syndrome,
retinitis pigmentosa–dysacusis
syndrome or
dystrophia retinae dysacusis syndrome...
- and
retinitis pigmentosa is a
condition related to
changes in
mitochondrial DNA.
Mutations in the MT-ATP6 gene
cause neuropathy, ataxia, and
retinitis pigmentosa...
- more sensitive.
Defects in the
rhodopsin gene
cause eye
diseases such as
retinitis pigmentosa and
congenital stationary night blindness.
Rhodopsin was discovered...
-
rhodopsin gene (RHO), the gene
encoding for
retinitis pigmentosa GTPase regulator (RGPR), and the gene
encoding retinitis pigmentosa 2
protein (RP2). Allelic...
-
Muscular atrophy-ataxia-
retinitis pigmentosa-diabetes
mellitus syndrome, also
known as Kurukawa-Takagi-Nakao
syndrome is a very rare
genetic disorder...
-
approved by the U.S. FDA in
August 1998, as a
treatment for
cytomegalovirus retinitis.
Several morpholino oligos have been
approved to
treat specific groups...
-
those who
suffer from
retinitis pigmentosa and
other degenerative eye diseases, and to find a cure for
those diseases.
Retinitis pigmentosa Macular degeneration...
