-
Oculocutaneous albinism is a form of
albinism involving the eyes (oculo-), the skin (-cutaneous), and the hair. Overall, an
estimated 1 in 20,000 people...
- this is
contrary to
definitions where the
condition is inherited.
Oculocutaneous albinism (OCA) is a
clearly defined set of
seven types of
genetic mutations...
-
Oculocutaneous albinism type I or type 1A is an
autosomal recessive skin disease. This
subtype of
oculocutaneous albinism is
caused when the gene for tyrosinase...
- albinism:
oculocutaneous,
affecting the eyes, skin and hair, and
ocular affecting the eyes only.
There are
different types of
oculocutaneous albinism depending...
-
dilution protein homolog, is a
protein that in
humans is
encoded by the
oculocutaneous albinism II (OCA2) gene. The P
protein is
believed to be an integral...
- (archived 9
October 2006, from the original,
accessed 18–22 July 2006). "
Oculocutaneous Albinism". NORD (National
Organization for Rare Disorders). Retrieved...
-
Oculocutaneous albinism immunodeficiency Oculocutaneous albinism type 1
Oculocutaneous albinism type 2
Oculocutaneous albinism type 3
Oculocutaneous albinism...
- is an
extremely rare
autosomal recessive disorder which results in
oculocutaneous albinism (decreased pigmentation),
bleeding problems due to a platelet...
- that
mediates melanin synthesis.
Mutations in this gene are a
cause of
oculocutaneous albinism type 4.
Alternative splicing results in
multiple transcript...
-
Ocular albinism is a form of
albinism which, in
contrast to
oculocutaneous albinism,
presents primarily in the eyes.
There are
multiple forms of ocular...
