Know the Early Symptoms of Angelman Syndrome in Children from an early age

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Angelman syndrome is a disorder that occurs due to genetic factors. This condition attacks the nervous system, causing sufferers to experience delays in the development process. People with Angelman syndrome may have physical and intellectual development problems. Angelman syndrome is congenital.

In fact, this disease is classified as rare and only occurs in 1 in 12 thousand people. The symptoms of Angelman syndrome often go unrecognized when a baby is born. Over time, the symptoms of this disease will slowly appear, usually at the age of 6-12 months. This condition is characterized by babies experiencing a delay in development and development when compared to babies their age.
Angelman Syndrome Symptoms and Complications
Angelman syndrome causes babies to develop delays in development. Symptoms will usually appear when the child enters the age of 6-12 months, one of which is not able to sit alone without assistance. Even though the age is increasing, the child's growth does not occur normally. Symptoms will become more apparent as the baby approaches 2 years of age, namely the size of the baby's head that is not developing as it should.

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Babies with Angelman syndrome have a smaller head size and are prone to seizures. In addition, this disorder is also characterized by several other symptoms, such as impaired balance and coordination, trembling arms, sticking out tongue, crossed eyes, light colored hair and eyes, but pale skin, and difficulty chewing and swallowing food.

This disease occurs because there is a genetic disorder. In the human body, there are copies of the UBE3A gene pair that are passed down from the father (paternal) and mother (maternal). In almost all parts of the body, these two genes will be active simultaneously. Unlike the brain, in some parts of the brain only one copy of the UBE3A gene is active, namely the maternal gene.

Also read: Must Know, Angelman Syndrome Diagnosis Procedures in Children

Angelman syndrome occurs due to missing or damaged copies of maternal genes that should be active. Angelman syndrome can also occur when a child inherits a pair of UBE3A genes on chromosome 15, but both come from a paternal gene (uniparental disomy). Unfortunately, until now it is not certain what causes the gene mutation to occur and trigger Angelman syndrome.
Have you ever heard of the term Angelman syndrome? This condition occurs when a child is born with a genetic disorder that affects the nervous system. This health disorder triggers developmental delays, especially intellectual problems. Not only that, children also often experience problems with speech development and impaired balance of body movements. So, what are the symptoms of Angelman syndrome in children that need to be known? Come on, read the full explanation below.
Angelman Syndrome in Children, These Are the Symptoms
As with other babies, people with this condition appear normal at birth into the world. But when he has entered the age of eating, he will experience interference. Children with Angelman syndrome also experience developmental delays at the age of 6-12 months. The symptoms of this one health disorder will vary for each child. Here are some symptoms to watch out for:

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Children are lazy to speak or don't even speak at all.
The child has impaired cognitive development, as well as intellectual.
Children have difficulty balancing body movements.
Children are often seen smiling and laughing for no reason.
Children have a passionate personality and are always fun.
Children experience sleep disorders, such as insomnia and lack of sleep.
The child has seizures.
The child has a protruding lower jaw shape.
The child has stiff legs.
The child is hyperactive or too active.
The child experiences sudden stiff or jerking movements.
The child has a sharp head.
The child has unusual behavior, such as raising his arm while walking.
The child has hyperpigmentation of the hair, eyes and skin.
Also read: Including Genetic Disorders, Know 5 Facts about Angelman Syndrome

For a more detailed explanation of the symptoms of Angelman syndrome in children, mothers can pay attention to the following things:

Ataxia. This condition is characterized by a lack of coordination between limbs. This is characterized by shaking when holding objects, walking, even while eating.
Tremor. Nerve disorders that occur in the body will cause tremors. Not only that, children will also experience anxiety and hyperactivity.
Scoliosis. This condition is characterized by the shape of the spine that curves to the side. The sign can be seen from the difference in the height of the right and left shoulders.
Cockeye. This condition occurs because the muscles around the eye are weakened, so the eyeballs are not aligned.