Albinism affects the production of melanin, the pigment that colours skin, hair and eyes. It’s a lifelong condition, but it doesn’t get worse over time.
People with albinism have a reduced amount of melanin, or no melanin at all. This can affect their colouring and their eyesight.
Albinism is caused by faulty genes that a child inherits from their parents.
Symptoms of albinism
Hair and skin colour
People with albinism often have white or very light blonde hair, although some have brown or ginger hair. The exact colour depends on how much melanin their body produces.
Very pale skin that burns easily in the sun and doesn’t usually tan is also typical of albinism.
How albinism is inherited
The two main types of albinism are:
- oculocutaneous albinism (OCA) – the most common type, affecting the skin, hair and eyes
- ocular albinism (OA) – a rarer type that mainly affects the eyes
Autosomal recessive inheritance
In most cases, including all types of OCA and some types of OA, albinism is passed on in an autosomal recessive inheritance pattern. This means a child has to inherit two copies of the faulty gene (one from each parent) to have the condition.
If both parents carry the gene, there’s a 1 in 4 chance that their child will have albinism and a 1 in 2 chance that their child will be a carrier. Carriers don’t have albinism but can pass on the faulty gene.
Some types of OA are passed on in an X-linked inheritance pattern. This pattern affects boys and girls differently: girls who inherit the faulty gene become carriers and boys who inherit the faulty gene will get albinism.
When a mother is a carrier of an X-linked type of albinism, each of her daughters has a 1 in 2 chance of becoming a carrier and each of her sons has a 1 in 2 chance of having albinism.
When a father has an X-linked type of albinism, his daughters will become carriers, and his sons won’t have albinism and won’t be carriers.
Read more about how mutations are passed on.
If you have a history of albinism in your family or you have a child with the condition, you may want to talk to your GP about getting a referral for genetic counselling.
A genetic counsellor provides information, support and advice about genetic conditions. For example, you can discuss with them how you inherited albinism and the chances of passing it on.
Read more about genetic testing and counselling.
Albinism is usually obvious from a baby’s appearance when they’re born. Your baby’s hair, skin and eyes may be examined to look for signs of missing pigment.
As albinism can cause a number of eye problems, your baby may be referred to an eye specialist (ophthalmologist) for tests to check for conditions such as nystagmus, squint and astigmatism.
Electrodiagnostic testing is also sometimes used to help diagnose albinism. This is where small electrodes are stuck to the scalp to test the connections of the eyes to the part of the brain that controls vision.
Treatments for eye problems due to albinism
Although there’s no cure for the eye problems caused by albinism, there are a number of treatments, such as glasses and contact lenses, that can improve vision.
A child with albinism may also need extra help and support at school.
Glasses and contact lenses
As a child with albinism gets older, they’ll need regular eye tests, and it’s likely they’ll need to wear glasses or contact lenses to correct problems such as short-sightedness, long-sightedness or astigmatism.
Vision aids include:
- large-print or high-contrast books and printed materials
- magnifying lenses
- a small telescope or telescopic lenses that attach to glasses to read writing in the distance, such as on a school whiteboard
- large computer screens
- software that can convert speech into typing or vice versa
- tablets and phones that allow you to magnify the display to make writing and images easier to see
The Royal National Institute of Blind People (RNIB) has more information about living with low vision, including a section on education and learning.
Photophobia or sensitivity to light
Sunglasses, tinted glasses and wearing a wide-brimmed hat outside can help with sensitivity to light.
There’s currently no cure for nystagmus (where the eyes move from side to side involuntarily). However, it isn’t painful and doesn’t get worse.
Certain toys or games may help a child make the most of the vision they have. An ophthalmologist will be able to provide further advice.
Surgery, involving dividing and then reattaching some of the eye muscles, may occasionally be an option. Read more about the procedure "tenotomy of horizontal eye muscles for nystagmus".
Squint and lazy eye
The main treatments for squints are glasses, eye exercises, surgery and injections into the eye muscles.
If your child has developed a lazy eye, they may benefit from wearing a patch over their “good” eye to encourage their other eye to work harder.
Read more about treatments for squints.
Reducing the risk of sunburn and skin cancer
If you have albinism, you should wear sunscreen with a high sun-protection factor (SPF). An SPF of 30 or more will provide the best protection.
It’s also a good idea to look out for skin changes, such as:
- a new mole, growth or lump
- any moles, freckles or patches of skin that change in size, shape or colour
Report these to your doctor as soon as possible. Skin cancer is much easier to treat if it’s found early.
Read more about protecting your skin and eyes from the sun.
Help and support
There’s usually no reason why someone with albinism can’t do well in normal schooling, further education and employment.
With appropriate help and support, most children with albinism can attend a mainstream school.
Speak to your child’s teacher if your child experiences bullying or name-calling because of their condition.
It may also help to talk to other people with albinism. The Albinism Fellowship has a contact person network that can provide advice and support locally.
National Congenital Anomaly and Rare Diseases Registration Service
If you or your child has albinism, your clinical team will pass information on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).
The NCARDRS helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.