What Is Horner's Syndrome?
Horner’s syndrome is an uncommon disorder, known as oculosympathetic paralysis, in which the nerves of the eye and face are affected. Due to this syndrome, the pupil of the affected side of the face contracts. Likewise, the eyelid droops and sweating on that side decreases.
Horner’s syndrome always occurs as a consequence of an underlying disease. The most common disorders that normally develop from it are:
- Tumor or lesion on the spinal cord
- Brain tumor
In certain situations, doctors might not be able to find the underlying condition that provokes it. In this case, it’s difficult to treat the syndrome, since treating the underlying cause is what could restore normal nerve functions.
You should keep in mind that Horner’s syndrome can occur in people of any age. Additionally, as we mentioned before, it’s not very common at all.
Why does it happen?
To understand why Horner’s syndrome happens, you have to look at the functioning of a series of nerve fibers, such as the fibers related to sweating, the pupils, and some muscles around the eyes.
These start in the part of the brain called the hypothalamus and go to the face and eyes. If the path of these nerve fibers is affected at any point then it gives rise to Horner’s syndrome.
The path these nerve fibers run is very complex. From the brain, they go down the spinal cord, they come out at chest height, and go back up through the neck next to the carotid artery. Then they go into the skull and arrive at the inside of the eye.
The damage caused to these nerve fibers can be caused by the following:
- A lesion on the carotid artery, one of the main arteries that goes to the brain.
- A lesion on the nerves at the base of the neck, called the brachial plexus.
- Flare-ups of migraines.
- Tumor, stroke, or other damage to the brain or in the brain stem.
- Tumor on the upper part of the lung.
- Sympathectomy. This is an injection or surgery to interrupt the nerve fibers and alleviate a specific pain.
There are certain cases in which Horner’s syndrome develops at the moment of birth. This affliction can cause a lack of color and pigmentation in the iris. Although this syndrome doesn’t have many cases, the congenital syndrome is estimated to affect 1 of every 6000 births.
Horner’s syndrome, depending on the location and the way the underlying condition occurs, can be classified in four different ways. Therefore, there is central, preganglionic, postganglionic, and congenital Horner’s syndrome.
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Symptoms of Horner’s syndrome
You should keep in mind that Horner’s syndrome only affects one side of the face. The most frequent signs and symptoms used to identify this affliction are the following:
- Falling of the upper eyelid.
- Slight raising of the lower eyelid.
- Miosis. That is, a continuously small pupil.
- Anisocoria. Which means there is a notable difference in the size of both pupils.
- Small or slow dilation of the pupil under the effect of a small light.
- Lessening, or lack of sweat on the affected side of the face.
These symptoms aren’t easy to detect. They can develop subtly, which complicates diagnosis of this syndrome.
Symptoms in kids
In cases where Horner’s syndrome develops in children, there are a series of characteristic symptoms that you can observe. The iris of the affected eye becomes lighter in color, especially in children under one year old.
Additionally, the affected side of the face doesn’t get red. The kid’s face should redden naturally from physical effort, emotional reactions, or heat. However, in the case of Horner’s syndrome, it doesn’t happen.
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Diagnosis and treatment of Horner’s syndrome
To diagnose the syndrome, professionals evaluate some of the following observable symptoms through an eye exam:
- Changes in contraction or dilation of the pupil
- Fallen eyelid
- Conjunctival injection
Treatment, as we mentioned before, depends on the original cause of the disorder. There isn’t a specific treatment for Horner’s syndrome. Doctors will proceed to treatment once they identify what caused it.
It’s worth mentioning that, when suffering this syndrome, the eyelid only falls a little. And this is the biggest obstacle to the patient’s daily life.
Additionally, there aren’t normally complications. Complications that can appear are often related to the underlying cause of the syndrome, or the treatment itself.