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Peutz-Jeghers syndrome - traducción al ruso

AUTOSOMAL DOMINANT GENETIC DISORDER CHARACTERIZED BY THE DEVELOPMENT OF BENIGN HAMARTOMATOUS POLYPS IN THE GASTROINTESTINAL TRACT AND HYPERPIGMENTED MACULES ON THE LIPS AND ORAL MUCOSA (MELANOSIS)

Peutz-Jeghers; Polyps-and-Spots syndrome; Hamartomatous intestinal polyposis; Polyposis, hamartomatous intestinal; Polyps-and-spots syndrome; Peutz-jeghers syndrome; Peutz-Jegher's syndrome; Peutz jeger; Jeghers-Peutz syndrome; Peutz-Jeghers syndrome; Polyposis hamartomatous intestinal; Peutz jegher; Peutz-jegher; Peutz-Jeghers polyp

Peutz-Jeghers syndrome

медицина

полипоз кишечника тип II

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

cerebro-oculo-facio-skeletal syndrome

RARE AND FATAL AUTOSOMAL RECESSIVE NEURODEGENERATIVE DISORDER

Cockayne's syndrome; Neiill-Dingwall syndrome; Neill-Dingwall syndrome; Dwarfism-retinal atrophy-deafness syndrome; Cockayne syndrome type 1; Cockayne syndrome type 2; Cockayne syndrome type 3; Cerebrooculofacioskeletal Syndrome; Cockayne Syndrome type II; COFS syndrome; Pena Shokeir II syndrome; Pena Shokeir syndrome type II; Cerebrooculofacioskeletal syndrome; Pena-Shokeir syndrome, type 2; Cockayne syndrome type A; Cockayne syndrome type B; Cockayne syndrome type C; Cockayne syndrome type III; Cerebro-oculo-facio-skeletal syndrome; Cerebrooculofacioskeletal syndrome 1; Cerebrooculofacioskeletal syndrome 2; Cerebrooculofacioskeletal syndrome 4; Cofs syndrome; Type II Cockayne syndrome; Pena-Shokeir syndrome type II; Cocaine Syndrome; Cocaine syndrome

медицина

церебро-окуло-фациоскелетный синдром

Definición

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.

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Wikipedia

Peutz–Jeghers syndrome

Peutz–Jeghers syndrome (often abbreviated PJS) is an autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis). This syndrome can be classed as one of various hereditary intestinal polyposis syndromes and one of various hamartomatous polyposis syndromes. It has an incidence of approximately 1 in 25,000 to 300,000 births.

https://en.wikipedia.org/wiki/Peutz–Jeghers syndrome

¿Cómo se dice Peutz-Jeghers syndrome en Ruso? Traducción de &#39Peutz-Jeghers syndrome&#39 al Ruso