Sneddon Syndrome: Causes, Symptoms, Diagnosis & Treatment
Sneddon syndrome is a rare and progressive condition that affects your blood vessels. It causes ischemic strokes in young adults and is a form of arteriopathy . According to medical professionals, the condition is characterised by a disease of the small to medium-sized arteries which can cause an elevation in the chances of blood clots developing in the arteries; especially the arteries that supply to the skin and brain).
The condition causes the development of livedo reticularis, which are net-like patterns of discolouration on the skin as well as neurological abnormalities. Most cases of Sneddon syndrome are sporadic, however, familial cases associated with autosomal dominant inheritance have also been reported , .
Sneddon syndrome is often categorised into two different types depending on whether an underlying cause has been identified (primary versus idiopathic), or whether certain symptoms of the autoimmune disease are present or not (aPL-positive versus aPL negative).
The condition is also termed as livedo reticularis racemosa and cerebrovascular accidents and Sneddon's syndrome .
The signs of the condition vary in accordance with its severity as well as the areas in your body that are affected by the syndrome. The condition is primarily recognised by the most common symptoms, which are, livedo reticularis, net-like patterns of discolouration on the skin and neurological abnormalities. According to studies, the average age for the onset of neurological symptoms is 39 years and livedo can develop from 29 years .
One of the most common symptoms of Sneddon syndrome is a stroke, which is a severe one too. You can identify the onset of stroke through the following signs :
In women, it can develop some specific signs such as
In rare cases, the condition has been known to show the signs of Raynaud's phenomenon, which is a widespread and mottled-purple discolouration on the body . And some of the others rare symptoms include chorea and myelopathies which are the disorders of the spinal cord, high blood pressure, heart disease, ophthalmologic (eye) complications, and impaired renal (kidney) function.
Studies have been unable to understand the exact reason behind the development of the condition. It is understood that Sneddon syndrome develops due to the changes in the CECR1 gene. The changes in the genes aid in producing the enzyme known as adenosine deaminase 2, which supports the lining of the blood vessel walls .
In some cases, the syndrome is associated with autoimmune diseases such as systemic lupus erythematosus, antiphospholipid syndrome, Behçet disease, or mixed connective tissue disease.
Genetic factors are also asserted to play a role in causing Sneddon syndrome. It is pointed out to be a cause as there have been reports of familial cases. It has been reported that the syndrome can affect more than one family member, such as the occurrence of it being on siblings. A person can carry the gene or genes of the syndrome without having any symptoms, as the condition will only be activated or triggered under specific circumstances .
The examination of the condition is carried out through physical examinations. The doctor will examine the medical history as well as the symptoms of the individual. You need to go to a doctor immediately in the event of livedo racemosa (pattern of skin discolouration).
The most commonly used diagnostic methods for Sneddon syndrome are skin biopsy and genetic tests. The neurological symptoms such as unexplained stroke in young individuals will also be examined by the doctor so as to understand the root cause of the severe symptoms .
Apart from these methods, the individual will have to undergo the following :
While conducting the blood tests to understand the symptoms, it will be used to examine the presence of the following :
As there is no cure developed for the condition, the treatment plans focus on managing the symptoms of the patient. The rare nature of the disease can be attributed to the lack of treatment methods developed. It is also the reason behind the lack of clinical studies conducted to further explore the condition and formulate a cure for it .
The treatment methods adopted for Sneddon syndrome are through blood thinning or anticoagulant medications such as warfarin. It helps in minimising the risk of stroke. If the individual is suffering from uncontrolled high blood pressure or diabetes or has the habit of smoking - the treatment methods will focus on dealing with those too. Some doctors suggest that it is preferable for patients who are aPL-negative to adopt methods that are lesser aggressive such as an approach consisting of antiplatelet therapy with aspirin , .
Angiotensin-converting enzyme (ACE) inhibitors are also employed as it can reduce the growth of the inside lining of the vessels (endothelial proliferation). Prostaglandin is employed to improve gas exchange and blood flow in the small vessels .
Refrain from smoking and oestrogen oral contraceptives as it can control the severity of the neurological symptoms , .
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