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Page 1
Klippel-Trenaunay-Weber syndrome.
Meine JG, Schwartz RA, Janniger CK. Meine JG, et al. Cutis. 1997 Sep;60(3):127-32. Cutis. 1997. PMID: 9314616 Review.
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and soft-tissue hypertrophy of an extremity. ...We will review the clinical features, etiology, assessment, and treatment of patients with Kli …
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bony and s …
Klippel-Trenaunay Syndrome.
John PR. John PR. Tech Vasc Interv Radiol. 2019 Dec;22(4):100634. doi: 10.1016/j.tvir.2019.100634. Epub 2019 Sep 23. Tech Vasc Interv Radiol. 2019. PMID: 31864529 Review.
Klippel-Trenaunay syndrome or KTS is a complex vascular syndrome associated with overgrowth occurring as a result of somatic mutations in the PIK3CA gene. ...
Klippel-Trenaunay syndrome or KTS is a complex vascular syndrome associated with overgrowth occurring as a result of somatic m …
Klippel-Trenaunay Syndrome.
Suda T, Katagiri A, Fujii H. Suda T, et al. Intern Med. 2023 May 1;62(9):1377-1378. doi: 10.2169/internalmedicine.0251-22. Epub 2022 Sep 28. Intern Med. 2023. PMID: 36171122 Free PMC article. No abstract available.
Klippel-Trenaunay syndrome.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet. 2000 Jul 31;93(3):171-5. doi: 10.1002/1096-8628(20000731)93:3<171::aid-ajmg1>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10925375 No abstract available.
[Klippel-Trenaunay-Weber syndrome].
Ugurlucan M, Yerebakan C, Alpagut U, Tireli E, Dayioglu E. Ugurlucan M, et al. Wien Med Wochenschr. 2008;158(13-14):402-4. doi: 10.1007/s10354-008-0545-8. Wien Med Wochenschr. 2008. PMID: 18677592 German.
Klippel-Trenaunay syndrome is an inherited disorder that is known to affect the venous system. Besides venous pathologies, arterial stenosis and aneurysmatic dilatations are extremely rare. In this report, we present a 7-year-old boy with Klippel-Trenaunay …
Klippel-Trenaunay syndrome is an inherited disorder that is known to affect the venous system. Besides venous pathologies, art …
Klippel-Trenaunay syndrome.
Berry SA, Peterson C, Mize W, Bloom K, Zachary C, Blasco P, Hunter D. Berry SA, et al. Am J Med Genet. 1998 Oct 2;79(4):319-26. Am J Med Genet. 1998. PMID: 9781914 Review.
Patients with Klippel-Trenaunay (KT) syndrome have a complex constellation of anomalies that includes cutaneous capillary malformation (usually on an affected limb), abnormal development of the deep and superficial veins, and limb asymmetry, usually enlargement. ...
Patients with Klippel-Trenaunay (KT) syndrome have a complex constellation of anomalies that includes cutaneous capillary malf …
Klippel-Trenaunay--Weber syndrome.
Ofodile FA. Ofodile FA. East Afr Med J. 1981 Apr;58(4):298-302. East Afr Med J. 1981. PMID: 6266801 No abstract available.
Klippel-Trenaunay-Weber syndrome.
Nielsen JR, Tschen EH. Nielsen JR, et al. Cutis. 1987 Jul;40(1):51-3. Cutis. 1987. PMID: 2822360 Review.
The Klippel-Trenaunay-Weber syndrome is a congenital angiodysplasia most often characterized by a triad of symptoms: varicose veins, port-wine cutaneous hemangiomas, and symmetrical hypertrophy of the affected limb. ...
The Klippel-Trenaunay-Weber syndrome is a congenital angiodysplasia most often characterized by a triad of symptoms: va …
Klippel-Trenaunay-Weber syndrome: orodental manifestations and management considerations.
Fakir E, Roberts T, Stephen L, Beighton P. Fakir E, et al. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Jun;107(6):754-8. doi: 10.1016/j.tripleo.2009.01.037. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009. PMID: 19464652 Review.
Klippel-Trenaunay-Weber syndrome is characterized by a triad of features, namely, vascular nevi, venous varicosities, and hyperplasia of hard and soft tissues in the affected area. ...
Klippel-Trenaunay-Weber syndrome is characterized by a triad of features, namely, vascular nevi, venous varicosities, a …
Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
Abdolrahimzadeh S, Scavella V, Felli L, Cruciani F, Contestabile MT, Recupero SM. Abdolrahimzadeh S, et al. Biomed Res Int. 2015;2015:786519. doi: 10.1155/2015/786519. Epub 2015 Sep 16. Biomed Res Int. 2015. PMID: 26451379 Free PMC article. Review.
The phakomatoses have been traditionally defined as a group of hereditary diseases with variable expressivity characterized by multisystem tumors with possible malignant transformation. The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatos …
The phakomatoses have been traditionally defined as a group of hereditary diseases with variable expressivity characterized by multisystem t …
1,540 results

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