-
Retinitis pigmentosa (RP) is a
member of a
group of
genetic disorders called inherited retinal dystrophy (IRD) that
cause loss of vision.
Symptoms include...
-
Urticaria pigmentosa (also
known as
generalized eruption of
cutaneous mastocytosis (childhood type): 616 ) is the most
common form of
cutaneous mastocytosis...
- also
known as
Hallgren syndrome, Usher–Hallgren syndrome,
retinitis pigmentosa–dysacusis
syndrome or
dystrophia retinae dysacusis syndrome, is a rare...
-
Dermatopathia pigmentosa reticularis (DPR) is a rare,
autosomal dominant congenital disorder that is a form of
ectodermal dysplasia.
Dermatopathia pigmentosa reticularis...
- Neuropathy, ataxia, and
retinitis pigmentosa, also
known as NARP syndrome, is a rare
disease with
mitochondrial inheritance that
causes a
variety of signs...
-
Prurigo pigmentosa is a rare skin
condition of
unknown cause,
characterized by the
sudden onset of
erythematous pa****s that
leave a
reticulated hyperpigmentation...
- UK,
including The
Comedy Store.
McCausland is
blind due to
retinitis pigmentosa. In
December 2024,
McCausland won the twenty-second
series of BBC's Strictly...
- sensitive.
Defects in the
rhodopsin gene
cause eye
diseases such as
retinitis pigmentosa and
congenital stationary night blindness.
Rhodopsin was
discovered by...
- X-linked
retinitis pigmentosa GTPase regulator is a GTPase-binding
protein that in
humans is
encoded by the RPGR gene. The gene is
located on the X-chromosome...
-
Muscular atrophy-ataxia-retinitis
pigmentosa-diabetes
mellitus syndrome, also
known as Kurukawa-Takagi-Nakao
syndrome is a very rare
genetic disorder which...
