SKINIPEDIA - Skin Diseases & Conditions: Albinism
Skin Diseases and Conditions: Albinism
What is Albinism?
The word “albinism” refers to a group of inherited skin conditions. People
with albinism have little or no pigment in their eyes, skin, or hair.
They have inherited altered genes that do not make the usual amounts of a
pigment called melanin. One person in 17,000 in the U.S.A. has some
type of albinism. Albinism affects people from all races. Most children
with albinism are born to parents who have normal hair and eye color for
their ethnic backgrounds. Sometimes people do not recognize that they
have albinism.
A common myth is that people with albinism have red eyes. In fact there
are different types of albinism and the amount of pigment in the eyes
varies. Although some individuals with albinism have reddish or violet
eyes, most have blue eyes. Some have hazel or brown eyes. However, all
forms of albinism are associated with vision problems.
People with albinism always have problems with vision (not correctable
with eyeglasses) and many have low vision. The degree of vision
impairment varies with the different types of albinism and many people
with albinism are “legally blind,” but most use their vision for many
tasks including reading and do not use Braille. Some people with
albinism have sufficient vision to drive a car.
Vision problems in albinism result from abnormal development of the
retina and abnormal patterns of nerve connections between the eye and
the brain. It is the presence of these eye problems that defines the
diagnosis of albinism. Therefore the main test for albinism is simply
an eye examination.
Skin Problems
While most people with albinism are fair in complexion, skin or hair
color is not diagnostic of albinism. People with many types of albinism
need to take precautions to avoid damage to the skin caused by the sun
such as wearing sunscreen lotions, hats and sun-protective clothing.
Types of Albinism
While most people with albinism have very light skin and hair, not all do. Oculocutaneous (pronounced ock-you-low-kew-TAIN-ee-us) albinism (OCA) involves the eyes, hair and skin. Ocular albinism (OA), which is much less common, involves primarily the eyes, while skin and hair may appear similar or slightly lighter than that of other family members.
Over the years, researchers have used various systems for classifying oculocutaneous albinism. In general, these systems contrasted types of albinism having almost no pigmentation with types having slight pigmentation. In less pigmented types of albinism, hair and skin are cream-colored and vision is often in the range of 20/200. In types with slight pigmentation, hair appears more yellow or red-tinged and vision may be better. Early descriptions of albinism called these main categories of albinism “complete” and “incomplete” albinism. Later researchers used a test that involved plucking a hair root and seeing if it would make pigment in a test tube. This test separated “ty-neg” (no pigment) from “ty-pos” (some pigment). Further research showed that this test was inconsistent and added little information to the clinical exam.
Recent research has used analysis of DNA, the chemical that encodes genetic information, to arrive at a more precise classification system for albinism. Four forms of OCA are now recognized – OCA1, OCA2, OCA3 and OCA4; some are further divided into subtypes.
- Oculocutaneous albinism type 1 (OCA1 or tyrosinase-related albinism) results from a genetic defect in an enzyme called tyrosinase (hence ‘ty’ above). This enzyme helps the body to change the amino acid tyrosine into pigment. (An amino acid is a “building block” of protein.) There are two subtypes of OCA1. In OCA1A, the enzyme is inactive and no melanin is produced, leading to white hair and very light skin. In OCA1B, the enzyme is minimally active and a small amount of melanin is produced, leading to hair that may darken to blond, yellow/orange or even light brown, as well as slightly more pigment in the skin.
- Oculocutaneous albinism type 2 (OCA2 or P gene albinism) results from a genetic defect in the P protein that helps the tyrosinase enzyme to function. Individuals with OCA2 make a minimal amount of melanin pigment and can have hair color ranging from very light blond to brown.
- Oculocutaneous albinism type 3 (OCA3) is rarely described and results from a genetic defect in TYRP1, a protein related to tyrosinase. Individuals with OCA3 can have substantial pigment.
- Oculocutaneous albinism type 4 (OCA4) results from a genetic defect in the SLC45A2 protein that helps the tyrosinase enzyme to function. Individuals with OCA4 make a minimal amount of melanin pigment similar to persons with OCA2.
Researchers have also identified several other genes that result in albinism with other features. One group of these includes at least eight genes leading to Hermansky-Pudlak Syndrome (HPS). In addition to albinism, HPS is associated with bleeding problems and bruising. Some forms are also associated with lung and bowel disease. HPS is a less common form of albinism but should be suspected if a person with albinism shows unusual bruising or bleeding.
Genetics of Albinism part of Albinism Article is here
Horrific ALBINO MURDERS video by National Geographics
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