Oculocutaneous albinism type 2
What is Oculocutaneous albinism type 2?
A form of oculocutaneous albinism characterized by variable hypopigmentation of the skin and hair, numerous characteristic ocular changes and misrouting of the optic nerves at the chiasm.
Other condition names
- OCA2
Inheritance type
Autosomal recessive
Prevalence
- Worldwide: 1-9 in 100,000
- United States: 1-9 in 100,000
Age of Onset
- Infancy
- Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.