Inherited Ataxia: Argentius Researchers discovered which are the main symptoms -

These are coordinating and balanced disorders that are usually manifested by 20 and 40 years.In dialogue with experts, the differences in neighboring countries and calls for diagnosis and medical treatment describe in detail

Herdystation Ataxia is a part of the nervous system disease.They prevent human body from clean control movements.

They are called "hereditary" because they go to children through jeans through jeans.They are rare diseases that are mainly affecting the cerebellum and scattered nerves, which eliminates balance and harmony.

Argentina's Serebelum has been published in a special magazine in a special magazine.

One of the authors is Marcelo Merello, a researcher at Konicet, a career for Flenn nurologologist and director of Buenos Aires University.

The second colleague is a neurologist and researcher in the Conniset, and an unusual motor service in the section of Neurology.

What are the most common symptoms of the genus?

Genetic Ataxias towards the body to imbalance with the balance of balance.

"Bus symptoms often include impossible when walking, processing and problems."

Other symptoms may also be: fatigue, double vision and writing problems.

Symptoms begin from childhood, but occur during the most common adolescents or young people.

"However, adults can represent some types of hereditary ataxia," said Dr.Rossi.

Diagnosis, basic species and difficulties

Researchers collected information from the whole country and several forms of antennas against anti-virus anti-virus.

It has left for a casual institution of the situation because of the cases of the cases of diseases of the natural resources.

Although researchers have several types of illness, the most common spinalical spinal and the Spanish model in Argentina.

Although more than 40 Stocershipos Ataaxis is SCA1 (ATX-ATXN1), SCA2 (ATX-ATXN2) and SCA3 (ATXN-ATXN3), Everlasting.

They also found differences with other countries.I am Argentina, Ardina, the most common features of spinocheblose, but, Brazil, but there is no Mexico.

"These differences in sharing can be because of the first result of the results and historical account," researchers have spoken.

This prevalence difference with other countries in the region is important for the management of a medical specialist.

An objective is to show that you need to know how much it is needed and how many patients with ataxia live.

There is no record of how many people have lost genetic air conditioning in the country, and that makes the problem serious.

"The lack of sound and epidemagic epidemagic to prevent reality of the problem of the problem," explain the authors.

In addition to the study found that between 65% and 82% of patients with hereditary ataxis do not reach definitively genetic diagnosis.

With modern technologies, including modern technologies, including the process of the tests, and requires a demonstration of mysterious life phase.

Another obstacle is the upper problem and charge to achieve a genete analysis."Plowing of inspections, depreciation and exchange of genetic references in the public private system.

Access to genetic tests in Argentina impedes several factors, including the increasing cost of limited insurance and reagent.The Neck family should wait for years to know the exact name of the disease.

The experts have been considered five tasks to make the people better to be careful with kindness and treatment:

- Apply cohort searches with the best technology

- Create a national register of ataxia patients

- ensure international contact

- Create social care

- To improve access to genetic tests

He said: they do not like the accompanying signs of their families and the healthy partnership with their families, they told them that they are accompanied by everyone who could work with the family.

Consultado por , el médico neurólogo Marcelo Kauffman, investigador del Conicet y jefe de la Unidad Neurogenética del Hospital Ramos Mejía de Buenos Aires, coincidió en que “los pacientes con ataxias hereditarias enfrentan todavía barreras para acceder a un diagnóstico genético, principalmente por las dificultades para obtener la financiación de los estudios a través de un sistema de salud fragmentado”.

EN 2020 Kaufman Xunto Con Josefina Pérez Maturo, Lucía Zavala, etc. Publicaron Un Cohorte, showed that the only unity of any inherited Ataxis patients, indirect diagnosis, with those with a family history, is an unimaginable face.

He is part of a doctor's doctor in the Medical Medical Medical Medical Medical Medical Medical Dr. Part of the Research Institute (iIMT), which is part of the research institute (iIMT), which is part of the research institute (iIMT), as part of the researcher (iIMT), as part of the researcher's research (iIMT), as part of the researcher's research (iIMT), as part of the researcher's research (iIMT), as part of the researcher's research (iIMT), as part of the researcher's research (iIMT), as part of the researcher's research.(IMIT), a part of the researcher, research in medical doctor, the Medical Medical Dr. Part of the researcher (iIMT), a research doctor in the Medical Dr.

"He said," he said, "he said," said that the importance of funding is possible to support groups of professionals and infrastructure that these families are important for dozens of families. "