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Maroteaux-Lamy syndrome - translation to russian

LYSOSOMAL STORAGE DISEASE

Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate; Maroteaux-Lamy syndrome; Mucopolysaccharidosis vi; Maroteaux-Lamy Syndrome; MPS VI; Maroteaux Lamy disease; Mucopolysaccharidosis VI; Mucopolysaccharidosis type VI; Mucopolysaccharidosis VI (Maroteaux-Lamy); MPS6; MPS 6; Maroteaux-Lamy; Mucopolysaccharidosis type 6; Polydystrophic dwarfism

Maroteaux-Lamy syndrome

медицина

дистрофическая дисплазия

мукополисахаридоз VI типа

синдром Марото-Лами

acrodysostosis

DYSOSTOSIS THAT RESULTS IN SHORTENING OF INTERPHALANGEAL JOINTS LOCATED IN HAND OR LOCATED IN FOOT ALONG WITH MENTAL DEFICIENCY

Maroteaux-Malamut syndrome; Arkless-Graham syndrome; Acrodysostosis syndrome

медицина

акродизостоз

adiposogenital dystrophy

HYPOTHALAMIC DISEASE THAT IS CHARACTERIZED BY ENDOCRINE DYSFUNCTION OF THE HYPOTHALAMIC GLAND RESULTING IN DELAYED PUBERTY, SMALL TESTES, AND OBESITY

Babinski-Fröhlich syndrome; Fröhlich's syndrome; Froelich's syndrome; Frölich's Syndrome; Launois-Cleret syndrome; Frölich's syndrome; Frohlich's Syndrome; Froelich's Syndrome; Fröchlich syndrome; Dystrophia adiposogenitalis; Babinski-Fröhlich disease; Adiposogenital Dystrophy; Frolich's syndrome; Frolich's Syndrome; Frohlich's syndrome; Froehlich's syndrome; Babinski-Froehlich syndrome; Babinski-Frohlich syndrome; Babinski-Froehlich disease; Babinski-Frohlich disease; Frochlich syndrome; Froechlich syndrome; Babinski–Fröhlich syndrome

медицина

гипофизарный евнухоидизм

адипозогенитальная дистрофия

гипофизарное ожирение

Definition

Reye's syndrome

['re?z, 'r??z]

¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.

Origin

1960s: named after the Australian paediatrician Ralph D. K. Reye.

Show more definitions

Wikipedia

Maroteaux–Lamy syndrome

Maroteaux–Lamy syndrome, or Mucopolysaccharidosis Type VI (MPS-VI), is an inherited disease caused by a deficiency in the enzyme arylsulfatase B (ARSB). ASRB is responsible for the breakdown of large sugar molecules called glycosaminoglycans (GAGs, also known as mucopolysaccharides). In particular, ARSB breaks down dermatan sulfate and chondroitin sulfate. Because people with MPS-VI lack the ability to break down these GAGs, these chemicals build up in the lysosomes of cells. MPS-VI is therefore a type of lysosomal storage disease.

https://en.wikipedia.org/wiki/Maroteaux–Lamy syndrome

What is the Russian for Maroteaux-Lamy syndrome? Translation of &#39Maroteaux-Lamy syndrome&#39 to R