What is Wolf-Hirschhorn Syndrome?

by time news

2024-04-10 23:07:03

It is possible that you have heard about this disorder, but do not know how it develops and what it consists of, that is why we share it with you. What is Wolf-Hirschhorn Syndrome.

It is necessary to know that this syndrome is characterized by the patient presenting typical craniofacial features, common in the nose, microcephaly, high forehead with prominent glabella, hypertelorism, arched eyebrows, thin upper lip or micrognathia.

In addition, it can also be identified that the patient has pre- and postnatal growth retardation, hypotonia and developmental delay, seizures, sleep problems. feedingintellectual disabilities.

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Patients may also have epilepsy and abnormalities that can affect other organs, so it is very important to see a specialist to provide the appropriate treatment for the patient.

after knowing What is Wolf-Hirschhorn Syndromeyou may be wondering what the causes of this condition are and here we share it with you.

What causes Wolf-Hirschhorn syndrome?

Experts reveal thatWolf-Hirschhorn syndrome It is recorded in one in every 50 thousand births and appears due to the lack of chromosome 4.

Likewise, it is reported that children who have this disorder are likely to survive into their twenties, since later the conditions could increase, until they become serious.

It is reported that this disorder is hereditary and is caused by the mutation of a gene found on chromosome 4, which is found in all cells of the body.

How is Wolf-Hirschhorn syndrome detected?

According to the study ‘Wolf-Hirschhorn syndrome: Report of a clinical case and review of the literature’, It is indicated that the diagnosis can be made by means of a conventional cytogenetic analysis.

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This analysis is capable of identifying the majority of cases that register this syndrome, which requires treatment with rehabilitation, speech therapy, antiepileptic drugs when necessary and feeding by gavaje or gastrostomy.

This disease can cause the wear and tear of some cells. nervous of the brain and is recorded when the patient is born with a defective gene, although symptoms can appear after age 30.

What part of the brain does Huntington’s disease affect?

This disease occurs due to the gradual degeneration of parts of the basal ganglia, better known as the caustic nucleus and putamen.

Take into account that the basal ganglia are groups of neurons that are found at the base of the braindeep in the brain and help smooth and coordinate each person’s movements.

At the moment there is no treatment that can help improve the quality of life of patients or affected people, although it can be supported with physical therapies, speech therapy, special education or medications.

now that you know What is Wolf-Hirschhor Syndrome and how you can identify it, we suggest you watch the following video:

#WolfHirschhorn #Syndrome

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