DefinitionThis section has been translated automatically.
An autosomal recessive form of oculocutaneous albinism type 2 (OCA 2) that only occurs in people with dark skin color: Medium brown hair, light brown skin, blue to brown iris. Photophobia and nystagmus slightly pronounced. No darkening in the course of life.
DiagnosisThis section has been translated automatically.
TherapyThis section has been translated automatically.
Recommended articles
Incoming links (1)
Albinism oculocutaneous tyrosinase-positive;Disclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
Prof. Dr. med. Peter Altmeyer