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ترجمة وتحليل الكلمات بواسطة الذكاء الاصطناعي
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%ما هو (من)٪ 1 - تعريف
Klippel–Trénaunay 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
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.
Reye's syndrome
SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS
Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; 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.
Frey's syndrome
HUMAN DISEASE
Auriculotemporal syndrome; Frey syndrome
Frey's syndrome (also known as Baillarger's syndrome, Dupuy's syndrome, auriculotemporal syndrome, or Frey-Baillarger syndrome) is a rare neurological disorder resulting from damage to or near the parotid glands responsible for making saliva, and from damage to the auriculotemporal nerve often from surgery.
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.
