Prader-Willi syndrome: how to suspect the symptoms of a genetic disease. Prader-Willi syndrome as a genetic pathology

Description:

Prader-Willi syndrome is a rare genetic anomaly. In Prader-Willi syndrome, approximately 7 genes from the 15th chromosome, inherited from the father, are absent or not expressed.

Karyotype 46 XX or XY, 15q-11-13. The disease was first described by Swiss pediatricians A. Prader and H. Willi in 1956.

According to the Prader-Willi Syndrome Association Registry, there were 1,595 patients in the United States and Canada as of December 1986. In recent years, it has been possible to establish a population frequency of pathology, which is 1: 10,000 - 1: 20,000.

Causes of Prader-Willi Syndrome:

The authors who first described the syndrome suggested an autosomal recessive mode of inheritance of the disease. Then there were reports of the possibility of autosomal dominant transmission of the disease. The observed family cases of pathology could serve as confirmation of these hypotheses. However, most of the described clinical observations of Prader-Willi syndrome were sporadic.

Subsequent studies made it possible to establish certain chromosomal abnormalities in children with Prader-Willi syndrome. Cytogenetic analysis showed that chromosomal abnormalities in patients were either translocations (t 15/15) or mosaicism. In 1987, the first reports of a microdeletion of chromosome 15 appeared. However, the final identification of chromosomal changes in Prader-Willi syndrome became possible only after the introduction of molecular genetic research methods into practice.

It has now been established that the development of Prader-Willi syndrome is associated with damage to the critical region of chromosome 15 (segment q11.2-q13). At the same time, it turned out that damage to the same region of chromosome 15 is also observed in another disease - Angelman syndrome, the clinical picture of which differs significantly from Prader-Willi syndrome and is characterized by an early (at the age of 6-12 months) slowdown in psychomotor development, microcephaly, speech impairment ( in 100% of cases), ataxia, uncontrolled violent laughter, frequent epileptiform seizures, a specific facial expression.

Thus, despite the damage in the Prader-Willi and Angelman syndromes of the same locus of chromosome 15, the clinical manifestations of both diseases are sharply opposite.

An explanation of phenotypic differences has been obtained only in recent years. It turned out that the development of these diseases is associated with new genetic phenomena - genomic imprinting and uniparental disomy.

Genomic imprinting is a new phenomenon discovered thanks to the advances in molecular genetics. It means different expression of genetic material (homologous alleles) in chromosomes depending on paternal or maternal origin, i.e. indicates the influence of parents on the phenotype of the child. Until now, it was believed that the contribution to the manifestation (expression) of the genes of the father and mother is equivalent.

In fact, genomic imprinting is a sexual and tissue-dependent complex modifier of the gene activity of some loci of chromosomes, depending on their parental origin. Manifestations of genomic imprinting have also been identified in other diseases - Sotos, Beckwith-Wiedemann, Silver-Russell syndromes, cystic fibrosis, and others.

Uniparental (uniparental) disomy - inheritance of both chromosomes from only one of the parents. For many years it was believed that such inheritance was impossible. Only with the help of molecular genetic markers was it possible to prove the possibility of uniparental disomy. The nature of uniparental disomy has not been completely elucidated, but it has been established that it owes its origin to a number of genetic and biochemical disorders.

It should be noted that it is impossible to detect a microdeletion or uniparental disomy using a conventional study of the chromosomal composition of the karyotype. For this, special cytogenetic and molecular genetic methods are used - prometaphase analysis, the use of DNA markers of certain sections of chromosome 15 (study of methylation processes), etc.

To date, the Prader-Willi and Angelman syndromes serve as a generally accepted model for studying new and complex phenomena in clinical genetics - genomic imprinting and uniparental disomy.

It has been established that Prader-Willi syndrome can be caused by two main mechanisms. The first of these is a microdeletion of chromosome 15 (15q11.2-q13), which is always of paternal origin. The second is maternal isodysomy, i.e. when both chromosomes 15 are from the mother. The development of Angelman syndrome, on the contrary, is associated with a microdeletion of the same region of chromosome 15, but of maternal origin, or paternal isodisomy. Most (about 70%) cases of Prader-Willi syndrome are due to microdeletion, the rest are due to disomy. At the same time, the absence of clinical differences between patients with microdeletion and isodisomia attracts attention.

Pathogenesis:

The pathogenesis of the Prader-Willi syndrome remains poorly understood to date. It is suggested that in patients it is due to a significant (more than 10 times) increase in fat synthesis from acetate and extremely low lipolysis processes.
according to the hypogonadotropic type, it can be associated with dysfunction of the hypothalamus, mainly in the region of the ventromedial and ventrolateral nuclei. The correctness of this point of view is confirmed by the effectiveness of the treatment of patients with pharmaceutical preparations (clomiphene), which led to an increase in plasma levels of luteinizing hormone, testosterone, normalization of renal excretion of gonadotropins, spermatogenesis, and the appearance of secondary sexual characteristics.

One explanation for hypopigmentation of the skin, hair, and iris is a decrease in tyrosinase activity in hair follicles and melanocytes, as well as a decrease in pigment in the retina.

Attention is drawn to the increased risk of leukemia in patients with Prader-Willi syndrome. Studies have revealed a decrease in DNA repair (up to 65% compared to 97% in a healthy child) in lymphocytes of patients with this pathology. It is possible that low DNA repair capacity can play a fatal role in the development of malignant neoplasms in individuals with Prader-Willi syndrome.

Symptoms of Prader-Willi Syndrome:

Children with Prader-Willi syndrome are usually born full-term with slight intrauterine malnutrition and often in. In 10-40% of cases, breech presentation is observed.

During the course of the disease, two phases can be distinguished: the first is characteristic of children 12-18 months of age. It is characterized by severe muscle hypotension, decreased reflexes - Moro, sucking and swallowing, which makes it difficult for the child to feed. The second - comes later, in a few weeks or months. Appear, a constant feeling of hunger, leading to the development of obesity, and the deposition of fat is observed mainly on the trunk and in the proximal limbs.

Muscular hypotension gradually decreases and almost completely disappears by school age. The feet and hands of patients are disproportionately small - acromicria. In children, hypogonadism is noted (in boys - hypoplasia of the penis, scrotum, and in girls - underdevelopment of the labia and in 50% of cases - the uterus).

The growth of patients is often reduced. In 75% of children, hypopigmentation of the skin, hair and iris is observed. Often diagnosed. Psychomotor development lags behind the age norm - the coefficient of intellectual development is from 20 to 80 units. (at a rate of 85-115 units). Speech is difficult, vocabulary is reduced. Patients are friendly, the mood is characterized by frequent changes. Disorders of coordination, strabismus are described.

There are other anomalies: microdontia, hypoplasia of the cartilage of the auricles, ectropion (eversion of the eyelid),.

Prader-Willi syndrome

Prader-Willi syndrome (abbreviated SPV)- this is rare in which seven (or some of their parts) on paternal chromosome 15 (Q 11-13) are removed or do not function normally (for example, with a partial deletion). The disorder was first described in 1956 Andrea Prader and Heinrich Willi, Alexis Labhart, Andrew Ziegler and Guido Fanconi.

PWS occurs in 1 in 25,000-10,000 newborns. It is very important to remember that the genetic material that affects the development of the disease is paternal. Because this region of chromosome 15 is characterized by the phenomenon of imprinting. And this means that for some genes in this region, only one copy of the gene functions normally, through

Human and mouse model studies have shown that deletion of 29 copies of the C/D box snoRNA SNORD116 (HBII-85) is the primary cause of Prader-Willi syndrome.

Diagnostics

PWS occurs in about 1 in 10,000 to 25,000 newborns. There are over 400,000 people worldwide who are living with PWS today. As already mentioned, this disease is traditionally characterized by hypotension, short stature, hyperphagia, obesity, and behavioral problems. Individuals with this disorder have small hands and feet, hypogonadism, and mild mental retardation.

However, if this disease is diagnosed at an early stage and its treatment is started, then the prognosis for the development of the disease becomes more optimistic. PWS, like autism, is a disease that has a very wide range of manifestations and signs. The course of the disease is different in each individual case and can vary from mild to severe, which progresses throughout a person's life. Prader-Willi syndrome affects various organs and systems.

Usually the diagnosis of Prader-Willi syndrome is made on the basis of clinical manifestations. However, genetic testing is increasingly being used today and is especially recommended for newborns with hypotension. Early diagnosis allows for early treatment of PWS. For children with the syndrome, daily injections are recommended. recombinant growth hormone (GH) . Growth hormone (hypophysis somatotropic hormone) maintains a constant increase in muscle mass and can reduce the patient's appetite.

The basis for the diagnosis of the disorder, as already mentioned, is genetic testing, which can be carried out by the α-methylation method, to determine whether there is a normally functioning region on chromosome 15q11-q13, deviations in which lead to Prader-Willi and Angelman syndromes. This test allows you to identify more than 97% of patients. Such testing is necessary to confirm the diagnosis of PWS, especially in newborns (since they are still very young to test their ability to diagnose the disease by clinical manifestations).

Since there are some difficulties in the birth of infants with Prader-Willi syndrome, it should be remembered that congenital trauma and oxygen deprivation can complicate genetic deficiencies, resulting in atypical PWS.

Differential Diagnosis

Often, Prader-Willi syndrome is misdiagnosed. The reason for this is that many doctors are not aware of this syndrome. It is sometimes considered Down's Syndrome because the disorder is much more common than PWS. In addition, obesity, which is characteristic of PWS, may also be present in Down syndrome through behavioral problems.

Adding to the problem is the fact that parents of children who have already been tested for Prader-Willi syndrome may tell friends, family, and even doctors and nurses that their child has Down syndrome, because more people know about this disorder. It is believed that about 75% of PWS remain undetected.

Treatment

There are currently no effective drugs to treat PWS. A number of drugs aimed at overcoming the symptoms of the disease are currently under development. During childhood, sick individuals should be treated to help improve muscle tone. Physiotherapy is very important. During the school year, sick children should receive extra help, and the learning process should be very flexible. The biggest problem associated with PWS is severe obesity.

Due to severe obesity, obstructive sleep apnea is a common complication, which is why it may often be necessary to use CPAP (individual medical device for automated long-term assisted intranasal ventilation of the lungs with constant positive pressure).

Society and culture

For the first time, public information about Prader-Willi syndrome appeared in the British media in July 2007, when the Channel 4 television channel showed a program called Can "t Stop Eating ("I can't stop eating"), which described the daily life of two people from SPV - Joe and Tamara.

Actress and neurologist Mayima Bialik wrote her thesis on Prader-Willi Syndrome for her PhD in 2008

In the process of intrauterine development, violations occur in the chromosome set of the child. In particular, they concern the functioning of the section q11-13 of the fifteenth pair. Answering the question of what it can be, and how the disease in question manifests itself in the future, experts always associate it with disorders at the level of paternal chromosomes.

Very often Prader-Willi syndrome is accompanied by:

• Deletion, that is, the complete loss of the Q 11-13 region of the father's gamete with a frequency of 70 cases out of 100.
• The absence of a copy of the fifteenth chromosome of paternal origin and the subsequent replacement of this copy by the maternal one with a frequency of 20 cases out of 100.
• Deactivation at the stage of embryonic development due to the mutation of the molecule and the preservation of the DNA nucleotide sequence with a frequency of 5 cases out of 100.

In the normal state, the copy of the gene received from the father should work, while the mother does not. Thus, the impossibility of solving natural problems due to the absence of this working copy can cause the development of the disease.

Symptoms

The first signs of the disease appear already at birth. The vast majority of babies diagnosed with Prader-Willi syndrome are born prematurely with obvious intrauterine malnutrition, i.e., atypically low mobility. Depending on the phase, the disease is characterized by:

• Muscle hypotension. Additionally, the syndrome is combined with the Moro reflex, insufficiency of tendon reflexes, and a tendency to hypothermia.
• Polyphagy. Vivid manifestations of the disease in the form of a constant feeling of insatiable hunger begin from the age of 6-12 months. Children with Prader-Willi syndrome are always obese. The deposition of subcutaneous fat occurs in the region of the proximal parts of the limbs, on the torso. The child's hands and feet remain small, out of proportion to the body. Hypotension in this phase is minimized.

Minor patients lag behind their peers in physical development. There is hypoplasia in the vulva - internal in girls - and cryptorchidism.

The psychomotor development of children diagnosed with Prader-Willi syndrome is somewhat abnormal. The child has excellent visual memory, learns to read quickly, but speech development is slow, vocabulary is limited. A minor patient has difficulty mastering mathematics and writing. He does not remember information well.

The list of symptoms can be supplemented:

• the presence of a high palate in the form of an arch;
• dryness of the mucous membranes of the oral cavity;
• microcephaly;
• damage to tooth enamel and caries;
• hypoplasia of the cartilaginous tissues of the ears;
• frequent convulsions and strabismus;
• curvature of the spine;
• coordination disorders;
• the presence of a transverse palmar fold.

All patients with Prader-Willi syndrome have:

• wide nose of large size;
• overweight with deposition of fat in the abdomen;
• increased sensitivity of the skin with instant bruising;
• disproportionately small hands and feet with narrow fingers.

Diagnosis of Prader-Willi syndrome in a child

The basis for the diagnosis is the symptoms of the disease, confirmed by genetic tests. In order to recognize the disease, the method of molecular genetic analysis or cytogenetic examination is used. In addition, doctors work with DNA markers for specific zones of the 15th and other chromosomes. It is impossible to diagnose the disease without resorting to these methods, in view of its similarity with others - for example, Down syndrome.

Complications

What is the danger of Prader-Willi syndrome? As a rule, it is not life-threatening, and the prognosis with treatment is favorable. The average life expectancy of patients is 60 years or more. Possible threats to health and life are:

• diabetes;
• leukemia.

Treatment

Taking into account the results of the diagnosis, doctors decide what to do to improve the quality of life of the child and contribute to his successful adaptation in society. It is completely impossible to cure the disease. And in order to prevent the consequences and minimize current symptoms, the course of treatment includes mainly physiotherapy - massage, exercise therapy, etc.

What can you do

Parents should treat the child together with doctors. Only under such conditions can we expect truly successful results. So, it is necessary to provide the patient with regular classes with a speech therapist and defectologist, training in groups or individual. When prescribing medication, you must follow the doctor's instructions.

What does a doctor do

A common practice is the appointment of hormone therapy. Hormone treatment consists of regular injections of "growth hormone". The introduction of gonadotropins can also be used to make up for the lack of their natural production. If the disease is accompanied by micropenia and undescended testicles in boys, hormone therapy may not be enough, and only surgery will help cure the symptom. In order to correct excess weight, the doctor prescribes a strict low-carbohydrate diet for the child.

Prevention

A congenital disease cannot be prevented. All that remains for parents to do is to prevent complications. The sooner a child receives treatment, the better his quality of life will be in the future. The child is capable of adapting to society, learning and interacting with others.

And caring parents will find on the pages of the service full information about the symptoms of Prader-Willi syndrome in children. How do the signs of the disease in children at 1.2 and 3 years old differ from the manifestations of the disease in children at 4, 5, 6 and 7 years old? What is the best way to treat Prader-Willi syndrome in children?

Take care of the health of your loved ones and be in good shape!

Prader-Willi syndrome is considered a very rare genetic disorder in which seven genes located on the 15th paternal chromosome are completely or partially absent and do not function normally.

This genetic pathology occurs due to the fact that only the copy of a certain gene received from the father functions correctly. There are also some irregularities in the copy from the mother. Let's consider in more detail.

In the body of a healthy person, there are copies of genes, thanks to which the organs can function without any deviations from the norm. With the development of Prader-Willi syndrome, such copies are absent. Currently known diseases that are inherently similar to this disease.

A similar mechanism of occurrence can also be observed in Angelman syndrome, but even in this case, mutations affect the genetic material received from the mother. Such diseases, as a rule, manifest themselves in various forms and have varying degrees of severity. However, they are incurable.

Causes of the syndrome

Prader-Willi syndrome is a hereditary deterministic pathology that develops only with the development of certain anomalies. In other words, with certain chromosomal disorders, parental genes begin to suffer, which leads to serious changes. The clinical picture develops when seven genes in the 15th paternal are absent or not expressed. In this case, the embedded information in DNA is not converted into RNA.

Scientists who were engaged in elucidating the causes of this hereditary pathology previously believed that a homozygote is formed due to such a deviation. Then it was concluded that the predominant traits are present in autosomes, and the main way of transmission of the disease is inheritance.

Geneticists carried out numerous pathologies, with the help of which it was found that the fathers of children affected by the disease had a translocation of chromosome 15. Photos of children with Prader-Willi syndrome are presented in our article.

genetic mechanism

To date, it has been precisely established that with this pathology, the 15th chromosome is damaged in segments from q11.2 to q13. The same thing happens with Angelman syndrome. However, this disease is characterized by completely different symptoms. Such a dissonance can only be explained by such a phenomenon in genetic science as genomic imprinting, as well as uniparental disomy.

In uniparental disomy, both chromosomes are inherited from only one parent, but for this to happen, certain biochemical factors must influence the gene material. This fact was established using prometaphase analyzes and DNA marking of some loci of this chromosome.

Prader-Willi syndrome is caused by two main mechanisms: microdeletion of the 15th chromosome, received from the father, and idiosomy of the maternal chromosomes, both of which are received from the mother.

With genomic imprinting, phenotypic changes depend on whose chromosomes - father or mother - have been expressed.

Prader-Willi syndrome in children

The mechanisms of disorders that occur in the body of a patient with a syndrome have not yet been fully studied. However, at the same time they have a number of symptoms inherent only to this type of disease. It is believed that patients gain weight due to an increase in the formation of fat cells and a decrease in the level of lipolysis.

In addition, there are dysfunctions of the hypothalamus, which are mainly noted in its two nuclei - ventrolateral and ventromedial. Such processes lead to failures in the formation of secondary sexual characteristics. Decreased tyronase activity in hair follicles and melanocytes results in hypopigmentation of the hair, skin, and iris.

What are the main symptoms of Prader-Willi syndrome?

Symptoms of the disease

This pathology can be detected even in the early stages of pregnancy with an incorrect location of the fetus and with its low mobility. In addition, the level of gonadotropin produced by chorion cells can change significantly in a pregnant woman, and symptoms of polyhydramnios may be present. Based on these symptoms, a diagnosis cannot be made, however, they may be a sufficient basis for further diagnosis.

Dysplasia

In children, Prader-Willi syndrome (pictured above) can be expressed in the presence of congenital dislocations of the hip (dysplasia), in weakening muscle tone, and also in coordination disorders. There are cases when a newborn could not suck and swallow breast milk on his own. In this violation, nutrition is carried out using a probe. Respiratory disturbances may occur, and in some cases mechanical ventilation of the respiratory system is required.

Drowsiness

In addition, there are other symptoms of Prader-Willi disease. For example, children may experience increased sleepiness. As for external factors, the child has developmental delays. Therefore, such patients are characterized by short stature, underdeveloped hands and feet, and strabismus often develops.

Other symptoms

In the future, this pathology is characterized by the following symptoms:

1. Curvature of the spinal column.
2. Caries of milk teeth and increased density of saliva.
3. Tendency to overeat.
4. Hypofunction of the gonads, which further lead to infertility.
5. Obesity.
6. Delayed motor and speech development.
7. Retardation in psychomotor development.
8. Delay in puberty.

These symptoms are determined visually. During adolescence, the following symptoms are detected:

Diagnosis of Prader-Willi syndrome

This hereditary pathology can be seen even during fetal development during ultrasound. In such cases, women are recommended certain types of prenatal diagnosis, and if necessary, specialists use invasive methods to solve the problem.

After childbirth, an experienced specialist has the right to make a diagnosis of Prader-Willi disease already at the initial examination of the baby. However, specific genetic testing is needed to confirm it. The content of chorionic gonadotropin is also examined in the mother's blood. Thanks to such methods, it is possible to identify submicroscopic and functional pathologies at the DNA level.

What are the criteria for diagnosis?

The diagnosis can be made according to the following clinical criteria:

1. At birth, low weight and height of the child in cases of full-term pregnancy.
2. Incorrect position, including breech presentation of the fetus.
3. Other microanomalies in development.
4. Expressed system.
5. Reduced pigmentation of the skin and hair.
6. Obesity, developing, as a rule, by six months.
7. Delays in psychological, motor and speech development.

Children who have this syndrome constantly require food and move very little. Due to excessive weight gain, they may experience such a complication as sleep apnea, which is often the cause of death in their sleep.

What is the treatment for Prader-Willi syndrome?

Treatment

To date, there are no specific treatments for the syndrome. Therapy is usually symptomatic. If a newborn has problems with respiratory activity, then he is transferred to artificial lung ventilation, and in case of problems with swallowing, they are put through which enteral nutrition is carried out. In cases of decreased muscle tone, massage and a variety of physiotherapy methods are indicated.

Children with Prader-Willi disease are given daily recombinant growth hormone, which maintains muscle mass gain and helps reduce the patient's appetite. The replacement of chorionic gonadotropin is also carried out.

During such a disease, hypogonadism is observed, that is, underdevelopment of the gonads and a change in the functions of the reproductive system. In this case, hormone replacement therapy is carried out, which allows to stimulate growth and puberty.

In some cases, children with speech delays and mental retardation may need the help of a psychiatrist or psychologist. And most importantly, it is necessary to constantly monitor the amount of food that they consume. Children with Prader-Willi syndrome are prescribed special diet therapy.

The risk that the second child of a couple whose first child suffers from this disease will be born with the same genetic problems is incredibly high. In such a case, parents are advised to undergo a consultation, where specialists will comprehensively examine them and calculate the risks.

Children with Prader-Willi disease need constant monitoring by an endocrinologist and a neurologist.

Improvement in general well-being against the background of the disease

Among people who have the syndrome, somatic morbidity rates are significantly increased, communication is difficult, and there is a need for specific assistance due to the characteristics of their disease. They may not understand why it is necessary to take care of their health. If the condition is satisfactory and the patient feels well, his quality of life improves.

The following factors must be eliminated:

1. Increased risk of sudden death.
2. The likelihood of getting sick.
3. An increase in the number of factors that determine material well-being.
4. Insufficient access to wellness and health services.

People with Prader-Willi pathology have special needs due to their underlying condition. They need special treatment for acute and chronic pathologies, assistance in strengthening general health, etc. Their needs must be met in special institutions providing medical care, which, in turn, may consist in the treatment of the underlying disease and somatic disorders, associated with the underlying pathology.

What is the life expectancy with Prader-Willi Syndrome? This disease often leads to a decrease in the life expectancy of patients up to 60 years. However, the prognosis for the recovery of such people is very disappointing.

The article presented a detailed description of the Prader-Willi syndrome. Now you know what this pathology is.

Prader-Willi syndrome is a genetic disease resulting from the appearance of a mutation in the 15th chromosome of the father.

Various options for changing the genetic material of the father, leading to the development of the disease (M - mother, O - father)

Anomalies include:

• deletion of a section of genes. This means that these genes were lost during the development of the germ cell. The probability of having two children with this pathology in a family is less than 1%.
• Maternal uniparental disomy (ORD). A child in the process of embryonic development receives two chromosomes from the mother and none from the father. The risk of a second anomaly in a second child is also about 1%.
• Imprinting mutation. In the presence of genetic material from both parents, the activity of the mother suppresses the expression of the father's genes, as a result, the child has only one functioning chromosome. The risk of re-mutation is up to 50%.

Note. In addition to Prader-Willi syndrome, there is a similar Angelman syndrome. The difference of this disease lies in the fact that the described violations occur not in the paternal, but in the maternal chromosome.

The pathogenesis of this disease is not fully understood, however, when analyzing the clinical picture, it was noticed that most of the symptoms result from dysfunction of the hypothalamus.

Clinical picture

The first symptoms of Prader-Willi syndrome appear before childbirth. The first signal is the presence of polyhydramnios. The diagnosis is made with the help of an ultrasound examination. The consequence of a large amount of amniotic fluid is the incorrect location of the child in the uterus.

Important! It must be remembered that, in addition to the Prader-Willi syndrome, a number of other diseases can cause polyhydramnios, for example, infectious diseases, Rhesus conflict, malformations, and more. This symptom is not highly specific.

In the neonatal period, the child will be lethargic, weak cry, poor sucking. All this is due to hypotension of the muscles.

Prior to the onset of puberty, Prader-Willi syndrome in children is manifested by a delay in mental and physical development. The child experiences learning difficulties, quickly gets tired.

At the age of 10-15 years, clinical symptoms become:

• delayed sexual development;
• hypogonadism;
• growth retardation;
• obesity.

Important! Most people with Prader-Willi syndrome have mild mental retardation (about 40%). 5% of patients have an average level of intelligence. 20% have borderline IQ values ​​between normal and delayed. Less than 1% suffer from severe mental retardation.

The cause of massive obesity is considered to be an increased level of ghrelin. This hormone is synthesized by the hypothalamus and is responsible for the feeling of hunger. The higher its level, the more you want to eat. People with Prader-Willi syndrome have several times the amount of ghrelin, which makes them prone to overeating.

Note. The first signs of obesity appear at the age of about 2 years.

Due to a malfunction of the hypothalamus, there is not sufficient stimulation of the pituitary gland, and the level of growth hormones and sex hormones is very low. This leads to infertility due to the underdevelopment of the reproductive system, as well as to the absence of a growth impulse.

Diagnostics

Despite the large number of symptoms, Prader-Willi syndrome is rarely diagnosed. According to statistics, about 2/3 of people with this genetic anomaly are left without a proper medical opinion.

The earliest diagnosis is made at the prenatal stage. However, it requires strict indications, for example, the presence of children or close relatives with this disease, polyhydramnios.

Important! Amniocentesis is an invasive diagnostic method that has a number of complications, including miscarriage or premature birth. Therefore, the need for this study must be carefully weighed.

The diagnosis of Prader-Willi syndrome is usually established clinically as early as around 10-12 years of age. By this time, a certain habitus (appearance) of the child is formed, and growth retardation and sexual development begin. The clinical diagnosis is confirmed by genetic analysis.

Treatment

Prader-Willi syndrome, like any genetic disease, is incurable. However, it is possible to reduce the manifestation of clinical symptoms and improve the quality of life of the patient. With an early diagnosis, correction of growth and sexual development begins with the help of synthetic analogues of somatotropin and sex hormones.

To combat muscle hypotension, physiotherapy and massage are performed. A nasal assisted ventilator is used to correct breathing problems, especially at night.

Important! Children should receive psychological support from their parents in matters of adaptation in the children's team and learning.

The life expectancy of people with Prader-Willi syndrome depends on various factors. First of all - from the amount of excess weight. On average, people suffering from this disease live up to 60 years or more, but obesity can lead to early death from cardiovascular diseases, as well as respiratory disorders. Therefore, people with this disease should be regularly observed by doctors and adhere to a strict diet.