Albinism refers to a group of rare inherited disorders that are present from birth. Albinism affects the amount of pigment found in the skin, hair, and eyes. People with albinism usually have little to no pigment in their eyes, skin, and hair. The degree of pigment loss can be quite variable. There are different types of albinism:
Albinism is caused by altered genes. The affected genes control the body's ability to make a pigment called melanin.
Altered genes are most often inherited from parents. Both parents will need to have the altered genes in order for the child to develop most types of albinism.
People can carry one set of altered genes and not have signs of albinism. They are called carriers. The second, healthy set of genes prevent the disease from developing.
Albinism is a hereditary disorder. People at risk of inheriting albinism are:
Albinism is rare. All races are affected, though Type 1 occurs predominantly in whites and Type 2 in blacks. Most children with albinism are born to parents with normal hair and skin color for their ethnic background.
The symptoms of albinism depend on the specific type of albinism. Some types affect the skin, hair, and eyes. Other types affect only the eyes or only the skin.
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Symptoms may include:
In many types of albinism, the disorder can be diagnosed by observing major or total absence of pigmentation of the hair, skin, and eyes and by vision problems. Most types of albinism affect the eyes. Certain eye tests (including an electroretinogram) are used to help confirm the diagnosis. For some types of albinism, DNA genetic testing can also be used to confirm the diagnosis.
While albinism is always visible at birth, it may be so mild that affected persons are unaware of their diagnosis unless abnormal eye movements or vision develop.
There is no cure for albinism. Treatment is aimed at preventing or limiting symptoms. In some cases, specific treatment for certain symptoms is needed.
Preventive treatment may include:
Specific treatment of symptoms for albinism may include:
Genetics Home Reference
National Organization for Albinism and Hypopigmentation (NOAH)
Canadian Dermatology Association
Canadian Ophthalmological Society
Hong ES, Zeeb H, Repacholi MH. Albinism in Africa as a public health issue. BMC Public Health . 2006 Aug 17;6:212.
Perry PK, Silverberg NB. Cutaneous malignancy in albinism. Cutis . 2001 May;67(5):427-30.
Rees JL. Genetics of hair and skin color. Annu Rev Genet . 2003;37:67-90.
Surace EM, Domenici L, Cortese K, Cotugno G, Di Vicino U, Venturi C, et al. Amelioration of both functional and morphological abnormalities in the retina of a mouse model of ocular albinism following AAV-mediated gene transfer. Mol Ther . 2005 Oct;12(4):652-8.
Last reviewed March 2013 by Brian Randall, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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