Early Symptoms The child has Angelman Syndrome

Early Symptoms The child has Angelman Syndrome



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.

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In fact, this disease is classified as rare and only occurs in 1 in 12 thousand people. Angelman syndrome symptoms often go unrecognized when the 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 developmental delays when compared to babies their age.

Angelman Syndrome Symptoms and Complications

Angelman syndrome causes babies to develop developmental delays. Symptoms will usually appear when the child enters 6-12 months of age, one of which is not being able to sit alone without assistance. Despite increasing age, the child's growth does not occur normally. Symptoms will become more visible as the baby approaches 2 years of age, namely the size of the baby's head that is not developing properly.

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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, protruding tongue, crossed eyes, light colored hair and eyes, but pale skin, and difficulty chewing and swallowing food.


This disease occurs because of a genetic disorder. In the human body, there are copies of the UBE3A gene pair that are inherited 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 there is only one active copy of the UBE3A gene, the mother gene.

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Angelman syndrome occurs due to missing or damaged copies of the mother's genes that are supposed to 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 this gene mutation and triggers 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, see the full explanation below.

Angelman Syndrome in Children, These are the Symptoms

Like other babies, people with this condition appear normal at birth into the world. But when he enters the age of eating, he will experience interference. Children with Angelman syndrome also experience developmental delays at 6-12 months of age. Symptoms of this one health disorder will vary for each child. Here are some symptoms to watch for:

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Children are lazy to talk or don't even speak at all.

The child has impaired cognitive development, as well as intellectual.

The child has hyperpigmentation in the hair, eyes and skin.

Children are often seen smiling and laughing for no reason.

The child has a protruding lower jaw shape.

Children have difficulty balancing body movements.

Children have passionate personalities and are always fun.

Children experience sleep disorders, such as insomnia and lack of sleep.

The child has a seizure.

The child has unusual behavior, such as raising his arm while walking.

The child has stiff legs.

The child is hyperactive or too active.

The child suddenly experiences stiff or jerky movements.

The kid has a sharp head.


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


Ataxia. This condition is characterized by a lack of coordination between limbs. It is characterized by shaking when holding objects, walking, even while eating.

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