7th World Congress on Human Genetics and Genetic Diseases
March 19-20, 2020 Dubai, UAE
April 08-09,2020 Sydney, Australia
13th International Conference on Genomics and Molecular Biology
May 25-26, 2020 Rome, Italy
Hunter syndrome, also called mucopolysaccharidosis II or MPS II, is a rare disease that's passed on in families. It usually affects only boys. Their bodies can't break down a kind of sugar that builds bones, skin, tendons, and other tissue. Those sugars build up in their cells and damage many parts of the body, including the brain. Exactly what happens is different for every person.
Large, round cheeks, Broad nose, Thick lips and a large tongue, Bushy eyebrows, Large head, Slowed growth.
Treatment: Due to the nature of the illness, and absence of a really efficient treatment, it is important to emphasize the need for extensive palliative treatment against the diverse symptoms. Their objective is to reduce the effects of the deterioration of many bodily functions. In light of the diversity of symptoms, it is quite common to use a wide spectrum of palliative strategies where surgery and therapies are often pivotal.
Stats: In contrast, others with Hunter syndrome develop severe mental impairment and have life expectancies of 15 years or fewer often due to neurodegeneration or physical complications from the disease. The age at onset of symptoms and the presence/absence of behavioral disturbances are predictive factors of ultimate disease severity in very young patients.