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Raynaud"s syndrome - tradução para Inglês
SYNDROME CHARACTERIZED BY CALCINOSIS, RAYNAUD'S PHENOMENO, ESOPHAGEAL DYSMOTILITY, SCLERODACTYLY AND TELANGIECTASIA
Crest syndrome; Calcinosis – Raynaud phenomenon – esophageal dysmotility – sclerodactyly – telangiectasia syndrome; Calcinosis–Raynaud phenomenon–esophageal dysmotility–sclerodactyly–telangiectasia syndrome; Calcinosis-Raynaud phenomenon-esophageal dysmotility-sclerodactyly-telangiectasia syndrome; Calcinosis - Raynaud phenomenon - esophageal dysmotility - sclerodactyly - telangiectasia syndrome; Limited cutaneous type scleroderma (systemic); Thibierge Weissenbach syndrome; Limited cutaneous systemic sclerosis; Limited systemic sclerosis/scleroderma; Limited systemic sclerosis; Limited systemic scleroderma; LcSSc; Thibierge-Weissenbach syndrome
![X-rays]] showing calcinosis in a woman with CREST syndrome.](https://commons.wikimedia.org/wiki/Special:FilePath/Calcinosis of CREST syndrome.jpg?width=200 "X-rays]] showing calcinosis in a woman with CREST syndrome.")
Raynaud's syndrome
n. Raynaud-Syndrom, Gefäßerkrankung (nach Maurice Raynaud benannt) von Gefäßkrämpfe gekennzeichnet
Maurice Raynaud
FRENCH DOCTOR (1834-1881)
A. G. Maurice Raynaud; Auguste Gabriel Maurice Raynaud
n. Maurice Raynaud (1834-1881), französischer Arzt der als erster das Raynaud-Syndrom in 1862 entdeckte und beschrieb
Turner syndrome
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![45,X [[karyotype]], showing an unpaired X at the lower right](https://commons.wikimedia.org/wiki/Special:FilePath/45,X.jpg?width=200 "45,X [[karyotype]], showing an unpaired X at the lower right")
![[[Histopathology]] of ovarian tissue in mosaic (A and B) and full (C) Turner syndrome](https://commons.wikimedia.org/wiki/Special:FilePath/Histological sections of ovarian cortex from patients with TS.png?width=200 "[[Histopathology]] of ovarian tissue in mosaic (A and B) and full (C) Turner syndrome")
![Height comparison for women with full and mosaic Turner's compared to [[trisomy X]] and the general population](https://commons.wikimedia.org/wiki/Special:FilePath/Relationship between chromosome X dosage in 45, X and 47, XXX females for quantitative traits.png?width=200 "Height comparison for women with full and mosaic Turner's compared to [[trisomy X]] and the general population")
CHROMOSOMAL DISORDER IN WHICH A FEMALE IS PARTIALLY OR COMPLETELY MISSING AN X CHROMOSOME
Turner's syndrome; Turner Syndrome; 45,X; XO syndrome; Turner's Syndrome; Gonadal dysgenesis Turner type; Bonnevie-Ullrich syndrome; Turners syndrome; Turners Syndrome; Karyotype 45,X; 45,X karyotype; Turner's; Turner disease; Ullrich-Turner syndrome; Bonnevie-Ulrich-Turner syndrome; Ulrich-Turner Syndrome; Bonnevie-Ullrich-Turner syndrome; Turner syndrome (Gonadal dysgenesis); Bonnevie Ullrich Turner syndrome; Single X syndrome; X syndrome; Bonnevie-Ulrich-Turner Syndrome; Bonnevie-Ulrich-Turner's Syndrome; Monosomy X; Partial anomalous venous drainage; Bonnevie–Ullrich–Turner syndrome; Bonnevie–Ullrich syndrome; Ring-X Turner Syndrome; Ring-X Turner syndrome; 45,X0
(Medizin) Turner Syndrom, genetisches Syndrom das hauptsächlich bei Frauen auftritt (rührt vom Fehlen des X-Chromosoms und führt zu Unfruchtbarkeit und weitere Erscheinungen)
Definição
Raynaud's disease
['re?n??]
(also Raynaud's syndrome)
¦ noun a disease characterized by whiteness, numbness, or pain in the fingers, typically brought on by constant cold or vibration.
Origin
C19: named after the French physician Maurice Raynaud.
Wikipédia
CREST syndrome
CREST syndrome, also known as the limited cutaneous form of systemic sclerosis (lcSSc), is a multisystem connective tissue disorder. The acronym "CREST" refers to the five main features: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia.
CREST syndrome is associated with detectable antibodies against centromeres (a component of the cell nucleus), and usually spares the kidneys (a feature more common in the related condition systemic scleroderma). If the lungs are involved, it is usually in the form of pulmonary arterial hypertension.
