Gaucher disease was first identified in 1882 by a French physician, Philippe Gaucher. It is a rare inherited metabolic disorder that results in the abnormal accumulation of certain types of lipids (fatty substances) in the spleen, liver, bone marrow, and lungs, and sometimes in the brain. This accumulation is due to either a deficiency or lack of an enzyme called glucocerebrosidase that is involved in the breakdown and metabolism of lipids, and more specifically glucosylceramide.

SUBTYPES OF GAUCHER DISEASE

Gaucher disease has been traditionally classified into three subtypes, depending on the symptoms and the timing of their development.

Type 1 Gaucher disease is the most common form of the disease. The mutation is most frequent in the Ashkenazi Jewish people. Type 1 Gaucher disease is also referred to as the adult or non-neuropathic form of Gaucher disease, in which the brain is not affected. People with type 1 Gaucher disease have an enlarged spleen and liver, anemia and a low platelet count, and may also experience bone pain and bone deterioration. Symptoms can appear at any age.

Type 2 Gaucher disease (infantile or acute neuronopathic) occurs rarely and shows no particular ethnic predisposition. Type 2 is the most severe form of Gaucher disease, with onset within the first 6 months of life, and a maximum life expectancy of about 2 years. Apart from splenic and liver enlargement, infants with type 2 Gaucher disease suffer extensive and progressive brain damage.

Type 3 Gaucher disease is common in the population of the Norbotten region of Sweden. It is also referred as juvenile or chronic neuronopathic Gaucher disease, because the neurological symptoms appear in early to late childhood. The neurological accumulation is often seen initially in children as problems with moving the eyes correctly, learning difficulties at school, or auditory problems, and may eventually lead to difficulty with movement and balance.


Recently, new clinical information have shown that type 1 Gaucher disease patients may also have some degree of neurological signs and symptoms, suggesting a continuum between neurologic and non-neurologic forms of Gaucher disease.

 

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Please note that the information contained in this section of the website is not intended for US residents. Please visit our US webpage.