«Әрнайы пәндер» бойынша терминологиялар стандарттарының жиынтығЫ

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• Тимома

Tay–Sachs disease — the most severe (and most common) of the lipid storage diseas- es, Tay–Sachs disease is characterized by neurological deterioration in the first year of life. It is caused by a genetic abnormal- ity on chromosome 15, which results in the deficient manufacture of lysosomal beta-hexosamindase A. As a result of this metabolic error, sphingolipids accumulate in the neural tissues of affected offspring. The illness is especially prominent in families of Eastern European (Ashkenazi) Jews. In this ethnic group it is carried by approximately 1 in 25 individuals. Carriers of the trait can be accurately detected by assay of hexosaminidase Тимома — айыршық бездің жасушалары- нан қалыптасқан ісіктердің жалпы атауы Тимома — опухоль тимуса, в половине слу- чаев т. вызывает сопутствующую тяжёлую псевдопаралитическую миастению; по кле- точной природе т. могут быть лимфоидными, эпителиальными, веретеноклеточными или смешанными; 2/ т. расценивают как добро- 3 качественные Thymoma — a rare neoplasm, usually found in the anterior mediastinum and originat- ing in the epithelial cells of the thymus. It is often associated with autoimmune dis- eases. Treatments may include surgical re- moval, radiation therapy, or chemotherapy жүктеу 0,76 Mb. Достарыңызбен бөлісу:

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