What is Coats Disease?
Coats Disease is a very rare condition where there is abnormal development in the blood vessels behind the retina of the eye. The blood-rich retinal capillaries break open, leaking the serum portion of the blood into the back of the eye. The leakage causes the retina to swell, leading to partial or complete detachment of the retina. Coats Disease progresses gradually and affects central vision. It is almost always unilateral (affecting only one eye). If caught early, some level of vision can typically be restored. If not treated until its later stages, complete loss of vision can occur. In the final stage, enucleation (removal of the affected eye) may be necessary.
Who is diagnosed with it?
It’s estimated that about 69% of the cases are male. The average age at diagnosis is 8–16 years, although the disease has been diagnosed in patients as young as 4 months. The peak age of onset is between 6-8 years of age, but ranges from 5 months to 71 years. About two-thirds of juvenile cases present before age 10 years; approximately one-third of patients are 30 years or older before symptoms begin. Coats Disease does not appear to be inherited and has no reported racial or ethnic predilection.
What are some of the early warning signs of this condition?
Yellow-Eye in Flash Photography. Just as the red-eye effect is caused by a reflection off blood vessels in the back of a normal eye, an eye affected by Coats will glow yellow in photographs as light reflects off cholesterol deposits.
Signs of loss of depth perception and parallax. When an eye is affected by Coats, the unaffected eye will often compensate for the loss of vision, resulting in some loss of depth perception and parallax.
A Yellow reflex from the pupil (called leukocoria)
Deterioration of sight in either the central or peripheral vision. This deterioration is likely to begin in the upper part of the vision field, as this corresponds with the bottom of the eye where blood usually pools.
The eye turning out or in (called strabismus)
What should I do if my child has symptoms of Coats Disease?
Don’t wait–talk immediately to your doctor about the possibility of Coats Disease. Time is of the essence for saving the eyesight. Recognizing early signs and knowing developmental milestones is important, and early intervention is key.
I think my child has Coats Disease, but neither my child’s pediatrician nor my child’s eye doctor has heard of it. What do I do?
You can start by making sure you have a reputable doctor and eye doctor on your side. Don’t stop there. Ensure that teachers, therapists, coaches, friends and family understand what the disease is and can respond to his/her needs appropriately. The JMCDF can help as a resource. Doctors on our website are available and have agreed to direct you to the nearest knowledgeable physician in your area. It helps enormously to plug into an already existing network of parents facing the same challenges as you, so utilize our website and message boards to communicate and find hope and answers.
When my child is being evaluated for Coats Disease, what signs are the doctor looking for?
Coats Disease is often misdiagnosed, so it is very important that you work with an ophthalmologist experienced in managing the disease. One challenge to making an accurate diagnosis is that the patients are often young people who can’t articulate their physical problem. Another is that the presenting symptoms of Coats can resemble other conditions such as retinoblastoma, which is potentially life-threatening.
By definition, patients with Coats Disease do not have any other health problems. However, symptoms that are typical of Coats may appear in several multisystem disorders, such as Fascioscapulohemeral Muscular Dystrophy, Pericentric Inversion of Chromosome 3, and Alport Syndrome.Again, One clue to a proper diagnosis is that Coats disease may be more often bilateral. As you can see, this is a complex disease to diagnose, and highlights once again the importance of working with physicians who are familiar with this condition.
What are the treatments available to my child?
(A sentence or two about what treatments are available and how they can help I.e., “Laser treatments can help stop leakage of the blood to the retina, which preserve eyesight.”
How many people in the United States are diagnosed with Coats Disease?
Less than 2000,000 people in the US population are affected. It’s listed as a “rare disease” by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). To put this in perspective, Ophanet, a consortium of European (physicians?) partners, currently defines a condition rare when if affects only one person per 2,000.
How did my child develop the disease?
No one knows. It’s still a mystery to retinal specialists. One possible clue is that it’s caused by a somatic mutation of the NDP gene. More study is required.
Is there a cure for this condition?
Unfortunately, experts have been unable thus far to come up with a cure for Coats Disease. Many treatments and therapies have surfaced to help the patient retain as much of their eyesight as possible, but no one yet has determined how to reverse the loss of eyesight.
Fortunately, with the advent of the Jack McGovern Coats Disease Foundation, there is hope for a reprieve and even a cure. Thus far, parents have been relying on early intervention by knowledgeable physicians to mitigate loss of eyesight. JMCDS is funding a select group of research scientists dedicated to finding a solution for this growing problem. The Foundation has also launched an outreach and fundraising campaign run entirely by volunteers, eliminating overhead and administrative costs.. Every dollar is supporting the efforts to find a cure. Current treatments have proven to be very successful, helping kids lead a full and active life, but JMCDS is holding out for more.
My child has just been diagnosed with Coats Disease. How do I cope?
First, be kind to yourself. It’s not easy to recover from the shock of learning your child has a disease that has no known cause or cure. Accept any and all feelings the diagnosis may elicit, and try not to blame yourself: It would’ve been impossible for you to figure out a way to shield your child from this disease.
The next step is to arm yourself with all the facts about the disease and understand that it is not a life threatening situation. Don’t let others write the end of your story. Many times the best intentioned people will say “there are many organizations to help with the blind.” Your child is not blind and rarely does the disease affect both eyes. Knowledge is power, and the more you know, the more capable you’ll feel about navigating the daunting healthcare system. That said, it’s also important to communicate with other patients and parents when it becomes too overwhelming. And if you find that the diagnosis has been so crippling that you’ve been unable to get past it, consider talking to a counselor or therapist. You can’t — and aren’t expected to — weather this storm alone.
Will my child be able to have a normal life? Attend school? Drive? Play sports?
Yes. Much depends on where your child falls on the spectrum, but with your support, as well as that of doctors, therapists and teachers, your child should be able to do everything a fully sighted child can do.