Klippel-Feil syndrome - significado y definición. Qué es Klippel-Feil syndrome
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Qué (quién) es Klippel-Feil syndrome - definición

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–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.

Wikipedia

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.