Gaucher's disease or Gaucher disease (GD) is a genetic disease where glucocerebroside (a sphingolipid, also called glucosylceramide) accumulates in cells and specific organs. The disease is characterized by swelling, tiredness, nausea, very low blood platelet augmentation and count of their liver and spleen, and is caused by a hereditary deficiency of the enzyme glucocerebrosidase (also referred to as glucosylceramidase), which functions on glucocerebroside. After the enzyme is faulty, glucocerebroside accumulates, especially in white blood cells and notably in macrophages (mononuclear leukocytes). Glucocerebroside can accumulate in the spleen, liver, kidneys, lungs, mind, and bone marrow.

Manifestations may include enlarged spleen and liver, liver malfunction, skeletal disorders or bone lesions which might be painful, acute neurological complications, swelling of lymph nodes and (sometimes) adjoining joints, bloated stomach, a brown tint to the skin, nausea, very low blood platelet count, along with yellowish fatty deposits on the white of the eye (sclera). Persons seriously affected are also more vulnerable to disease. Some kinds of Gaucher's disease might be treated with hormone replacement therapy.
Gaucher (go-SHAY) disease is the result of a buildup of certain fatty substances in certain organs, particularly your spleen and liver. This causes these organs to enlarge and can affect their function.

The fatty substances also can build up in bone tissue, weakening the bone and increasing the risk of fractures. If the bone marrow is affected, it can interfere with your blood's ability to clot.

 An enzyme that breaks down these fatty substances doesn't work properly in people with Gaucher disease. Treatment often includes enzyme replacement therapy.
An inherited disorder, Gaucher disease is most common in Jewish people of Eastern and Central European descent (Ashkenazi). Symptoms can appear at any age.

Symptoms

There are various kinds of Gaucher disease, and symptoms and signs of illness vary widely, even in exactly the exact same type. Type 1 is undoubtedly the most frequent.

Siblings, even identical twins, even together with the disorder can have various degrees of severity. Some folks who have Gaucher disease have only mild or no signs.

Most of us who have Gaucher disease have varying amounts of the following issues:

Skeletal abnormalities. Gaucher disease can weaken bone, raising the possibility of painful fractures. Additionally, it may interfere with the blood flow to your bones, which can lead to parts of the bone to die.

Blood disorders. A drop in healthy red blood cells (anemia) may lead to acute fatigue. Gaucher disease also affects the cells responsible for clotting, which may result in easy bruising and nosebleeds.

Abdominal complaints. Because the liver and especially the spleen can enlarge dramatically, the abdomen can become painfully distended.

More infrequently, Gaucher disease affects the brain, which may lead to abnormal eye movements, muscle rigidity, swallowing problems as well as seizures. 1 uncommon subtype of Gaucher disease starts in infancy and generally leads to death by two decades old.

Causes

Gaucher disease is passed along in an inheritance pattern called autosomal recessive. Both parents must be carriers of a Gaucher changed (mutated) gene for their child to inherit the condition.


Source: https://aderonkebamidele.com/gauchers-disease-causes-symptoms/