| KF | Kenner-fecal medium; kidney function; Klippel-Feil [syndrome] |
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| KFS | Klippel-Feil syndrome |
| KTS | Klippel-Trenaunay syndrome |
| KTW, KTWS | Klippel-Trenaunay-Weber [syndrome] |
| KTWS | Klippel-Trenaunay Weber syndrome |
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| Klippel | Maurice, French neurologist, 1858-1942. See: Klippel-Feil syndrome, Klippel-Trenaunay-Weber syndrome. (05 Mar 2000) |
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| klippel-feil syndrome | <syndrome> Fused vertebrae, especially cervical spine (C3-C4), elevation of scapula (Sprengel deformity), omocervical bones, GU abnormalities (66%), renal agenesis (33%), deafness (33%) (12 Dec 1998) |
| Klippel-Trenaunay-Weber syndrome | <syndrome> A congenital malformation syndrome characterised by the triad of asymmetric limb hypertrophy, haemangiomata, and nevi. Asymmetric limb hypertrophy is enlargement of one limb and not the corresponding limb on the other side, the enlarged limb being 3 times more likely to be a leg than an arm in ktw; and the limb enlargement is of bone as well as soft tissue. The haemangiomas, abnormal nests of blood vessels that proliferate inappropriately and excessively, cover a remarkable range from small innocuous capillary haemangiomas ( strawberry marks ) to huge cavernous haemangiomas. The nevi are pigmented moles on the skin; in ktw there are often also dark linear streaks on the skin, streaks due to too much pigment. There can be other abnormalities but the triad is the consistent clinical centrepiece of the disease. most persons with ktw have an enlarged leg and do relatively well without treatment or, for example, with only compression from an elastic stocking. Skin ulcers and other skin problems can occur over the swollen leg. Usually, the treatment is conservative. Surgery is almost never needed. The only possible exceptions are the very rare situations in which the leg reaches gigantic proportions or secondary clotting difficulties arise (due to trapping and destruction of blood platelets in a huge haemangioma). Then, amputation may become necessary. The cause of ktw syndrome is unknown. (12 Dec 1998) |
| syndrome, klippel-feil | The combination of short neck, low hairline at the nape of the neck and limited movement of the head. It is due to a defect in the early development of the spinal column in the neck (the cervival vertebrae). The condition is also called the klippel-feil sequence (referring to an embryologic or early developmental sequence of events). (12 Dec 1998) |
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| syndrome, klippel-trenaunay-weber | A congenital malformation syndrome characterised by the triad of asymmetric limb hypertrophy, haemangiomata, and nevi. Asymmetric limb hypertrophy is enlargement of one limb and not the corresponding limb on the other side, the enlarged limb being 3 times more likely to be a leg than an arm in ktw; and the limb enlargement is of bone as well as soft tissue. The haemangiomas, abnormal nests of blood vessels that proliferate inappropriately and excessively, cover a remarkable range from small innocuous capillary haemangiomas ( strawberry marks ) to huge cavernous haemangiomas. The nevi are pigmented moles on the skin; in ktw there are often also dark linear streaks on the skin, streaks due to too much pigment. There can be other abnormalities but the triad is the consistent clinical centrepiece of the disease. most persons with ktw have an enlarged leg and do relatively well without treatment or, for example, with only compression from an elastic stocking. Skin ulcers and other skin problems can occur over the swollen leg. Usually, the treatment is conservative. Surgery is almost never needed. The only possible exceptions are the very rare situations in which the leg reaches gigantic proportions or secondary clotting difficulties arise (due to trapping and destruction of blood platelets in a huge haemangioma). Then, amputation may become necessary. The cause of ktw syndrome is unknown. (12 Dec 1998) |
Synonyms : Dystrophia Brevicollis Congenitas, Klippel Feil Syndrome, Syndrome, Klippel-Feil
Synonyms : Disease, Klippel-Trenaunay, Klippel Trenaunay Disease, Klippel Trenaunay Weber Syndrome, Syndrome, Klippel-Trenaunay-Weber
| Klippel-Feil syndrome |
Klippel-Feil syndrome is a rare disorder characterized by the congenital fusion of any 2 of the 7 cervical (neck) vertebrae. It is caused by a failure in the normal segmentation or division of the cervical vertebrae during the early weeks of fetal development. The most common signs of the disorder are short neck, low hairline at the back of the head, and restricted mobility of the upper spine. ...
출처: en.wikipedia.org/wiki/Klippel-Feil_syndrome
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| Klippel-Weil sign |
flexion and adduction of the thumb when the patient's flexed fingers are quickly extended by the examiner; indicative of pyramidal tract disease.
출처: www.merckmedicus.com/pp/us/hcp/thcp_dorlands_conte...
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| Klippel-Feil syndrome |
A birth defect where two of the vertebral bones in the neck are joined together, this is associated with a higher than average incidence of disc disease.
출처: www.lieberson.com/en/neurgosurgery_glossary/k.htm
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| Klippel-Weil s. |
flexion and adduction of the thumb when the patient's flexed fingers are quickly extended by the examiner; indicative of pyramidal tract disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Klippel's disease |
[Maurice Klippel, Fr. neurologist, 1858?1942] Weakness or pseudoparalysis due to generalized arthritis.
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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