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Light micrograph of a section through the spleen of a patient with Gaucher's disease. Small lymphocytes and large macrophage cells (Gaucher?s cells, pink, a type of white blood cell) are present. Gaucher's disease is an inherited metabolic disorder in which a fatty substance called glucocerebroside accumulates in the spleen (in macrophages), lungs, liver and bone marrow, and sometimes the brain. This is due to an absence of the enzyme glucocerebrosidase (GC). The disease appears in childhood, and some forms are fatal in the first few years. Other forms cause enlargement of the affected organs, weak and painful bones and anaemia. Some forms also cause severe nervous system damage. There is no cure, but enzyme replacement therapy using GC can relieve the symptoms. Haematoxylin-eosin saffron (HES) stain. Magnification: x400 at 24x36 mm size.

Genes for Gaucher disease may have protected Jewish people against TB

6 February 2023

Gaucher disease, a genetic condition that is more common in Ashkenazi Jewish people, may confer protection against tuberculosis, according to research in zebrafish

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