Rett syndrome is an uncommon condition that affects the brain. It is a genetic condition and a developmental disorder that inhibits the proper growth of the brain. This leads to a worsening loss of motor skills and basic functions like speech. The condition most often affects young girls, although it can affect boys as well.
Most infants who have inherited the syndrome usually begin their lives quite normally. Although signs begin to show at around 6 months, for the first year and a half, they essentially grow at a normal pace, learn to crawl and walk properly, and begin to communicate normally. Unfortunately, usually around the year and a half mark, babies with Rett syndrome begin to lose the skills that they developed during their early age. The motor and mental degeneration continues and babies often become unable to properly function. There are other symptoms associated with the condition as well. Some babies will experience things like seizures and serious cognitive impairment. These problems can make it difficult or impossible for these young children to engage in healthy social activities.
There is no known cure for Rett syndrome; however, researchers are currently hoping to find healthy treatments. Currently, the best way to manage the problem is to work with therapists and kinesiologists who can help the children learn to control their movements, their speech, and their cognitive development. It’s also very important to make sure that the child has a healthy, supportive atmosphere in which they can grow. If you think that your baby is beginning to develop Rett syndrome, it’s a good idea to make sure that you’ve properly identified the symptoms. In this article, we’ve outlined the 10 most common symptoms of Rett syndrome. If you think your child is developing the condition, it’s best to seek help from your local healthcare provider.
Symptom #1: Stunted Growth
Babies with Rett syndrome often experience stunted growth in various areas. Usually, this begins as an abnormally slow growth of the brain after they are born. It’s normal for babies with the condition to have heads that are noticeably smaller than average.
As the child ages, it’s normal for them to experience stunted growth in other areas. They may have small extremities or be very short.