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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:

• Oculocutaneous albinism
  • Type 1—complete absence of pigment. Skin, hair, and eyes lack all pigment from birth. Freckles or moles will not appear at any time during their lifetimes. This group is divided into several subtypes depending on associated characteristics.
  • Type 2—decreased pigment, but may still have freckles and moles. This form of albinism is more common among persons of African descent. This form may be associated with such minor pigment loss that it is noticed only by looking at differences among other non-affected family members.
  • Both Type 1 and Type 2 albinism are usually associated with visual problems including nystagmus (abnormal jumping movements of the eyes) and decreased visual acuity, which is frequently not fully improved with glasses or contact lenses.
  • Type 3—reddish brown skin, reddish hair, and hazel or brown eyes, generally black South Africans.
  • Type 4––similar to type 2, predominantly in Japanese persons.
• Ocular albinism––an X-linked albinism where there are vision problems without changes in skin or hair.
• Hermansky-Pudlak––in addition to albinism, persons also have lung, bowel, and bleeding problems.
• Chediak-Higashi––in addition to albinism, persons also have immune problems with defects in the immune system.

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:

• Children of parents who have albinism
• Children of parents who do not have albinism, but carry the altered genes that cause this disorder
• A positive family history for albinism in a sibling or other relative

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.

Eye Symptom—Strabismus

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Symptoms may include:

• Eye problems, such as:
  • Strabismus or crossed or wandering eye
  • Poor vision (which usually cannot be fully corrected with glasses or contacts)
  • In some cases, functional blindness
  • Nystagmus or irregular, rapid eye movement.
  • Amblyopia or “lazy” eye.
  • Photophobia–sensitivity to bright lights or glare
• Skin problems, including:
  • Little or no pigmentation (resulting in extremely light or white skin)
  • Extreme sensitivity to sunburn
  • Very high susceptibility to skin cancer
• Hair problems, including:
  • White hair
  • Lighter than expected hair (often the forelock) being white
• Certain rare types of albinism, such as Hermansky-Pudlak syndrome, can cause other symptoms.

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.

There is no known way to prevent albinism. If you have albinism or have a family history of the disorder, you can talk to a genetic counselor when deciding to have children to understand the risks to your offspring.