Russell-Silver Syndrome: Causes, Symptoms And Treatment
Russell-Silver syndrome is a very rare congenital condition. That is, it is a disorder that comprises a set of symptoms and signs present from birth.
These children are characterized by growth retardation, both in the prenatal period and after delivery. In addition, they usually present body asymmetry that can affect the extremities and the face.
The abnormalities that usually appear in this syndrome can significantly compromise the life of those who suffer from it. Therefore, in this article we explain everything you need to know about Russel-Silver syndrome and how it can be treated.
What is Russell-Silver syndrome?
Russell-Silver syndrome is a rare disease. According to an article published in Orphanet , more than 500 cases have been described. However, no new ones have been published for a long time.
It is defined as a polymalformative disorder. This means that it produces malformations in different parts of the body. However, it has variable clinical expressiveness. There are mild cases, in which there are hardly any alterations, and other very serious cases in which life is compromised.
What happens is that, during the embryonic period, there is a delay in growth. These children usually have characteristic features. For example, asymmetry in the extremities or disproportion between the size of the head and the body.
The disease has no treatment as such. You can only try to reduce the impact that malformations have on the functionality of the person. That is why it is essential to know how to detect it early.
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