Gaucher Disease

I learned to never be quick to judge a person when you never know what a person is going through! Gaucher disease is a receivable inherited lysosomal storage disease. This characterization makes tone by bruising of bones because they are weak and derive of pain. The sickness that deliberates fatigue, anemia that undergoes pain, low blood platelet count that will be harder flowing, and growth of the liver and spleen. These visceral and neurologic symptoms are causing disruption of the lysosomes because of accumulation. The accumulation will cause damage to the organs such as spleen, liver, and brain. As we all know the location of lysosomes are in the cell that contains enzymes that digest and separate the cell after its death. The hereditary deficiency, meaning that it passes along with the families of the enzyme glucocerebrosidase which act on glucocerebroside that will collect.
Gaucher disease develops and partially reproduce to act as a molecular chaperone. This approach will direct and allow outgrowth of influence to get rid of certain fats. If the fat builds up, it can cause problems in the body which leads to the neurologist and visceral symptoms. I read in the article that there are typically three types of Gaucher’s disease. Type one is the most common disease and the symptoms may be mild, moderate, or severe. Type two affects the brain and spinal cord which is awful because that is where the storage of the nerves is. The nerves are a major component dealing with the body because it sends and receive information and allows our cells to communicate with each other. Type three is the same as type two, but it usually shows up later in the years. This can be dangerous because there’s no cure. It is best to get treated right