Синдром Аарскога – extremely a rare genetic disorder. This syndrome It leads to a change size and shape some bones and cartilages body. Often id=”result_box” lang=”ru”> the exposed face, fingers hands and feet.
Syndrome Aarskoga It is hereditary disorder. It caused gene mutation the X chromosome. It can be transmitted Mother-to- male children.
Риску заболевания синдромом Аарскога подвержены в основном мужчины. Болезнь передается от матери, у которой есть ген данного заболевания, ребенку мужского пола.
Основными симптомами синдрома Аарскога являются:
Непропорционально маленький рост;
Отклонения формы головы и лица, including:
Other symptoms may include:
Диагностика синдрома Аарскога обычно основана на лицевых особенностях больного. Правильность диагноза может быть подтверждена рентгеноскопическим снимком лица и черепа.
Currently, there is no no known method for a complete cure syndrome Aarskoga. Treatment limited surgery treatment states, caused disorder. Such treatment often it brings good results. Studies have established, that the syndrome Aarskoga cause gene disruption FGD1. Genetic testing for mutations of the gene may identify predisposition to disease.
Treatment includes:
Surgical intervention, Indications for the treatment of these disorders:
Orthodontics
In some cases, Orthodontic treatment can help when anonomaliyah person and dental anomalijax.
Support typically includes Help for depression, suffering mental disorders. Parents of children, syndrome patients Aarskoga also often require counseling and psychological support.
There is no way to prevent the disease syndrome Aarskoga. Genetic studies can only identify a predisposition to the disease.
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