Noun
/mænəˈsoʊdɪsɪs/
Mannosidosis is a rare genetic disorder characterized by the accumulation of mannose-containing oligosaccharides in the body due to a deficiency in the enzyme alpha-mannosidase. This disorder leads to various health issues, including neurological problems, skeletal deformities, and immune system dysfunction. The term is primarily used in medical and scientific contexts, often within discussions related to genetics, biochemistry, and pediatric medicine.
In terms of frequency, the term "mannosidosis" is used infrequently in everyday conversation but appears more often in academic literature, medical reports, and specialized discussions among healthcare professionals. Its usage is predominantly written, given the technical nature of the subject.
Example Sentences: 1. The patient was diagnosed with mannosidosis after genetic testing confirmed the deficiency of enzymes. - El paciente fue diagnosticado con mannosidosis después de que las pruebas genéticas confirmaron la deficiencia de enzimas.
La mannosidosis a menudo es mal diagnosticada debido a sus síntomas complejos que se asemejan a los de otros trastornos genéticos.
Researchers are studying new treatment options for individuals affected by mannosidosis.
While "mannosidosis" is a highly technical term and does not commonly appear in idiomatic expressions, its contextual embeddings mainly occur in medical literature rather than in colloquial language. Therefore, idiomatic expressions are not prevalent.
The term "mannosidosis" is derived from the combination of "mannose," a type of sugar, and the suffix "-osis," which is used in medical terminology to denote a pathological condition. The term encapsulates the biochemical basis of the disorder, indicating the accumulation of mannose derivatives in the body.
Synonyms: - None commonly used; it is a specific medical term.
Antonyms: - There are no direct antonyms, as "mannosidosis" refers to a specific condition rather than having counterparts in a more generalized sense.
Mannosidosis is an important term within the context of genetic and metabolic disorders, underscoring the significance of proper enzyme functioning in human health.