Albinism

Albinism is a congenital condition caused by a gene defect. This gene defect results in a lack or reduced ability to form the pigment melanin in eyes, skin and hair.
Published:
23/8/2024

What is

Albinism (from Latin albus , meaning white ) is a congenital condition in which the skin, hair and eyes lack the pigment melanin in whole or in part.  

People with albinism thus lack the sun-protective effect of melanin, and therefore have a significantly increased risk of sun damage and sun-related disease. Many are also visually impaired due to disturbances in the development of the eyes.  

There are approximately 250-300 people with the condition in Norway.


What is due

The condition is caused either by an error in the conversion of the amino acid tyrosine into the pigment melanin (so-called tyrosinase deficiency) or other enzyme errors.

Most forms of albinism are inherited in an autosomal recessive manner. This means that people with albinism have inherited a disease-causing gene from both father and mother.


How to treat

There is no treatment for albinism. However, it is very important to have good sun protection and specialist follow-up (dermatologist and ophthalmologist).

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Our dermatologists help people of all ages, from newborns to the elderly, with everything from simple skin changes to serious conditions.

Jon Anders Halvorsen
Mari Skylstad Kvernebo
Michael Zangani
Katarina Zak Stangeland
Jürgen Funk
Elin Holthe Johnsen
Bjørnar Halsør Moen
Thomas Schopf
Linnea Randisdatter Torsnes
Nils-Jørgen Mørk
Kim Endre
Carl Fredrik von Krogh
Mohammad Rizvi
Trine Lilly Halvorsen
Xiaotong Li
Roza Garvik
Christian Vestli
Christoffer Aam Ingvaldsen
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Nerea Bratteland
Henrik Aasrum Svendsen
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