Klippel-Trenaunay-Weber syndrome - tradução para árabe
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Klippel-Trenaunay-Weber syndrome - tradução para árabe

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
  • [[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome

Klippel Trenaunay Weber 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
‎ مُتَلاَزِمَةُ كليبل-ترينونيه -ويبَر:وحمة ضخمة في أحد الأطراف‎
Klippel-Trenaunay-Weber 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
مُتَلاَزِمَةُ كليبل-ترينونيه -ويبَر (وحمة ضخمة في أحد الأطراف)
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
‎ مُتَلاَزِمَةُ كليبل-ترينونيه:وحمة ضخمة في أحد الأطراف‎

Definição

Weber
(a.) A name suggested by Clausius and Siemens to denote a magnet pole of unit strength. This use is abandoned. (b.) It has been used to designate the unit of quantity--the coulomb. This use is abandoned. (c.) It has been used to designate the unit of current strength the ampere. This use is abandoned. [Transcriber's note: Definition (a) is now used. One weber of magnetic flux linked to a circuit of one turn produces an electromotive force of 1 volt if it is reduced to zero at a uniform rate in 1 second.]

Wikipédia

Klippel–Feil syndrome

Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck (cervical vertebrae).: 578  It results in a limited ability to move the neck and shortness of the neck, resulting in the appearance of a low hairline.

The syndrome is difficult to diagnose, as it occurs in a group of patients affected with many different abnormalities who can only be unified by the presence of fused or segmental cervical vertebrae. KFS is not always genetic and not always known about on the date of birth.

The disease was initially reported in 1884 by Maurice Klippel and André Feil from France. In 1919, in his Doctor of Philosophy thesis, André Feil suggested another classification of the syndrome, encompassing not only deformation of the cervical spine, but also deformation of the lumbar and thoracic spine.