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Klippel-Trenaunay syndrome - ترجمة إلى الروسية
Klippel-Trenaunay syndrome
SYNDROME THAT IS CHARACTERIZED BY LARGE CUTANEOUS HEMANGIOMATA WITH HYPERTROPHY OF THE RELATED BONES AND SOFT TISSUES
Klippel-Trénaunay-Weber; Klippel-trenaunay-weber syndrome; Klippel Trenaunay Weber syndrome; Klippel Trenaunay syndrome; Klippel-Trenaunay-Weber; Klippel-Trenaunay-Weber Syndrome; Klippel-Trenaunay-Weber syndrome; Klippel-Trénaunay-Weber Syndrome; Klippel–Trenaunay syndrome; Angioosteohypertrophy syndrome; Hemangiectatic hypertrophy; Klippel-Trenaunay syndrome; Klippel-Trénaunay-Weber syndrome; Klippel–Trenaunay–Weber syndrome; Klippel-Trenaunay Syndrome; Klippel–Trénaunay–Weber syndrome; Klippel-Trénaunay syndrome
хирургия
синдром Клиппеля-Треноне
Klippel-Feil syndrome
![[[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome](https://commons.wikimedia.org/wiki/Special:FilePath/Klippel–Feil syndrome and Sprengel's deformity.png?width=200 "[[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome")
PHYSICAL DISORDER THAT HAS MATERIAL BASIS IN ABNORMAL SEGMENTATION OF THE VERTEBRA DURING FETAL DEVELOPMENT WHICH RESULTS IN FUSION LOCATED IN CERVICAL VERTEBRA
Klippel Feil syndrome; Klippel-Feil anomaly; Klippel-feil syndrome; Klippel Feil; Klippel Feil syndrome dominant type; Klippel Feil syndrome recessive type; Cervical vertebral fusion; Cervical vertebral fusion, congenital; Congenital cervical vertebral fusion; Fused cervical segments, congenital; Congenital fused cervical segments; Klippel-Feil malformation; Klippel-Feil sequence; Klippel-Feil deformity; Feil-Klippel syndrome; Klippel-Feil anomalad; Klippel-Feil phenotype; Klippel-Feil syndrome; Frontonasal dysplasia klippel feil syndrome; Frontonasal dysplasia Klippel–Feil syndrome; Short neck syndrome; Klippel–Feil syndrome recessive type; Klippel–Feil syndrome dominant type; Frontonasal dysplasia Klippel-Feil syndrome; Klippel-Feil syndrome dominant type; Klippel-Feil syndrome recessive type; Klippel Feil Syndrome; Klippel–Feil Syndrome; Klippel-Feil Syndrome; Andre Feil
неврология
синдром Клиппеля-Фейля
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
تعريف
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.
ويكيبيديا
Klippel–Trénaunay syndrome
Klippel–Trénaunay syndrome, formerly Klippel–Trénaunay–Weber syndrome and sometimes angioosteohypertrophy syndrome and hemangiectatic hypertrophy, is a rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb.
