Achromatopsia is a non-progressive and hereditary visual disorder which is characterized by the absence of color vision, decreased vision, light sensitivity, and nystagmus. The cause of this disorder is absence of functioning cones (photoreceptors) in the retina. Patients with achromatopsia are only able to perceive black, white and gray shades colors. Their world consists of different shades of grey ranging from black to white, rather like only seeing the world as black and white.
What are the types of Achromatopsia?
Achromatopsia has two types; the complete type in which there is no functional cones in the retina at all and patients will have severe visual symptoms. The incomplete type in which there is some functional cones and patients will have less severe visual symptoms than the complete type.
What does a child with Achromatopsia have?
Children with achromatopsia will have reduced vision (20/200 or less), no color vision (they perceive only black, white and gray shades), sensitivity to light (photophobia) and the presence of nystagmus (shaking of the eyes). Achromatopsia is sometimes called ‘Day Blindness’, as these children see better in subdued light. Children with incomplete Achromatopsia may have better vision (20/120 to 20/80) and usually have less visual symptoms. Moreover, children may show paradoxical constriction of the pupil in the dark, usually have high hyperopic refractive errors (need for plus power glasses). Nystagmus and photophobia, marked in infancy, may improve with age. Achromatopsia is a non progressive disorder.
How common is Achromatopsia?
This condition affects approximately one in 40,000 live births. Its prevalence varies in different parts of the world. Because there is a genetic link, it is more common in regions where there is a high rate of consanguineous marriages (marriages between relatives) and in the eastern Pacific islands of Pingelap (see the book, ‘The Island of the Colour blind’ by Dr Oliver Sacks).
Are red-green color blindness and Achromatopsia the same condition?
No, red-green color blindness patients have difficulty distinguishing red and green colors. People with red-green color blindness have otherwise normal visual acuity and they do not have complete lack of color perception, instead they can perceive other colors.
What causes Achromatopsia?
Achromatopsia is a genetic disorder in which a child is born with nonfunctioning cones. The cones are special photoreceptor cells in the retina that absorb different color lights. There are three types of cones that are responsible for normal color vision. These are the red cones, the green cones, and the blue cones. A balanced distribution of these cells is necessary for normal color vision. A child born with non-functioning cones will have achromatopsia. There are several known genes mutations to cause achromatopsia and these are CNGA3, CNGB3, GNAT2, PDE6C.
How is the diagnosis made?
The diagnosis will be made by your ophthalmologist. Initially, symptoms such as light sensitivity and reduced vision will provide clues essential to the diagnosis. The retinal examination may in fact be normal. The color vision tests commonly performed in the clinic are the Ishihara pseudoisochromatic tests, H-R-R tests and the City University tests. The diagnosis can be confirmed by a specialized test called electroretinography (ERG) which usually confirms the diagnosis by showing specific waveforms shape. Genetic testing can be performed to test for the mutations in the most common genes. Also, new advances in retinal imaging gives Ophthalmologists better tools to evaluate the condition.
What are the chances of having more children with Achromatopsia?
Normally, each gene in the body has two copies, one copy comes from the mother and the other copy comes from the father. Achromatopsia is an autosomal recessive disorder, which means that for the disease to develop the two copies of the gene should be mutated.
Person who has only one gene diseased will not develop the disease because the other copy is working fine. This state is called a carrier. For a person to develop achromatopsia he must inherit one diseased copy from the mother and one disease copy from the father. Both parents must be carriers or diseased. This gives a family with one affected child a 25% (1 in 4) risk of each pregnancy carrying an affected offspring. There would also be a 50% chance that a child could be a carrier.
What treatment is available for Achromatopsia?
Currently there is no cure for achromatopsia. Research on gene therapy is ongoing and may lead to clinical treatments in the future. Animal models of achromatopsia in dogs and mice have shown promising results in restoring some cone function in the retina. Children should be checked for refractive errors (need for glasses). Prescribing glasses to correct refractive conditions such as far-sightedness (hyperopia), near-sightedness (myopia) and astigmatism can improve the vision somewhat but will not restore normal levels of vision. Red colored lenses help reduce the sensitivity to light and thus enhance visual functioning. NoIR (injection-molded) plastic wrap-around glasses have a top ‘shield’ that covers the top of a prescription frame as well as broad side shields which is important since stray light can be disabling. Examples are Corning Lenses: CPF 550 lenses (5% transmission, darkened) and CPF 550XD lenses (4% transmission, darkened). These lenses are available through Winchester Optical. A newer device known as an eyeborg can help people with no color vision to perceive color through sound waves. Artist Neil Harbisson who suffered from achromatopsia was one of the first to use this device.
How will this condition affect my child’s schooling?
With adequate help from teachers for the visually impaired, children with achromatopsia are usually able to attend mainstream schools. Front seat placement, large print books, and magnifying devices can be very helpful. A low vision evaluation will be necessary before school begins. More severely affected individuals may benefit from services available in schools specifically designated for the visually impaired.
Is there an Achromatopsia support group?