Rett S Syndrome

Rett syndrome is a rare genetic disorder that occurs predominantly in girls. It is characterized by slow development and regression of previously acquired skills, such as speech and purposeful movements, leading to severe disability.

Typical symptoms of Rett syndrome are:

1. Slowing of head growth after 6-18 months of life.

2. Loss of previously acquired speech and motor skills between 1 and 4 years of age.

3. Development of stereotypical hand movements such as squeezing, rubbing, clapping.

4. Problems with gait, scoliosis, tremor.

5. Intellectual impairments of varying severity.

6. Lack of eye contact, social withdrawal.

7. Epilepsy attacks, sleep disturbances, breathing and chewing problems are possible.

Girls with Rett syndrome require comprehensive medical and social care. Treatment is mainly symptomatic and supportive. Early diagnosis and stimulation of child development are important. The prognosis is generally serious, but life expectancy can be normal with adequate supportive care.

Rett syndrome is a rare genetic disorder that affects the brain and physical development of a person. The first symptom of Rett syndrome is muscle weakness. As the disease continues to progress, the child becomes increasingly clumsy and vulnerable. Before the discovery of the genetic cause of Rett syndrome, doctors considered it one of the “disorders with disorders.” This description clearly indicates a developmental disorder. In the modern world, it is recognized as a syndrome, as it is clearly designated as a species. The disorder is a genetic mutation that can occur in both boys and girls. Children with Rett syndrome are usually born healthy. They are of normal height and weight at birth. However, they begin to develop very quickly until the disorder manifests itself. Seizures begin within a few weeks of birth. Symptoms appear closer to 6 months after the onset of seizures. The most common symptoms are related to the position of the head on the arm. Because of this, speech disorders are often detected in such children. Strabismus is also a characteristic feature of Röth Syndrome. If you suspect your child has the syndrome, contact your doctor. He will be able to accurately diagnose the disorder and prescribe appropriate treatment.

Rett syndrome is a rare inherited disorder that affects the brain in girls.

It is a genetic condition, meaning it is passed on from mother to daughter. It causes the destruction of neurons and leads to brain damage, which manifests itself in a number of symptoms, such as:

1. Stereotypical movements are repeated and repetitive movements of the arms and body. Girls may begin to repeat any actions such as chewing, sucking or eating their own hair. These movements can be intrusive and constant, causing frustration and stress for those around the child.

2. Social isolation - Girls with Rett syndrome may avoid all contact with other people, including parents and teachers. They may sit at home alone without any communication or isolate themselves in their room.

3. Intellectual disability: Many girls with this condition have mental retardation because their brain stops working properly. However, this condition can be treated and improved with certain medications and therapies.

Rett syndrome affects various aspects of life, including learning, social interactions, and emotional stability. It can significantly impact the quality of life of the child and those around him.

Treatment for Rett syndrome may vary depending on the severity of the condition. Some of the treatments include medications, exercise, and behavioral therapy. It is important that treatment begins as early as possible and that parents and teachers are trained to effectively care for a child with this condition.

Good afternoon, dear readers! Today I would like to tell you about Rett syndrome, which is not often mentioned in our media.

Rett syndrome is a rare genetic disorder that occurs predominantly in girls, as it is characteristic of the X chromosome syndrome. This disorder is characterized by the presence of characteristic movements that appear in childhood and persist throughout life. In simple terms, Rett syndrome can be described as a progressive loss of interest in the world around us and social isolation.

The syndrome was first identified in 1966 during medical genetic examinations. Identifying signs of the disease has been difficult because numerous studies of syndromes that appear at such a young age are very similar in symptoms. The diagnosis of Rett syndrome was carried out thanks to genetic DNA data - diagnostics that confirmed the development of this particular type of Syndrome.

The main symptoms of the disease are: - Lack of interest in the environment; - Difficulty learning new skills, such as writing, reading or counting; - Loss of motor activity; - Impaired speech and communication skills; - Disturbances in the functioning of the brain associated with the inability to process information from the outside through the senses.

Symptoms of this disorder in girls are expressed already in childhood - in the fourth or fifth year of life. This leads to difficulties with self-care, as well as problems with learning at school. When symptoms worsen, they appear in adulthood, complications arise in the intestines, and the quality of care and digestion also deteriorates.

Often when diagnosing Ret syndrome

At the moment, Rett syndrome is extremely common. It manifests itself during the life of girls. Typically, this disorder can be diagnosed in the first year of life. In medical circles, this syndrome is called X-linked recessive retbonogen syndrome. Moreover, it can manifest itself either before the birth of the child, or in the first months of his life. One in ten thousand newborn girls will have this disease. But there are certain variations of this disorder. Over time, this disease is becoming more common. It occurs when chromosomes are arranged in a certain way. Sometimes other chromosomal features are observed. Many people believe that this disorder is hereditary. But the cause of this syndrome has not yet been established. This means that the exact cause of this disease cannot be identified.