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Year Number of Results
1972 1
1974 1
1979 1
1983 1
1984 2
1985 1
1987 2
1988 3
1989 2
1990 1
1992 1
1993 2
1994 4
1995 2
1996 3
1997 4
1998 2
1999 1
2000 7
2001 4
2002 1
2003 6
2004 5
2005 3
2006 4
2007 8
2008 2
2009 8
2010 8
2011 5
2012 2
2013 3
2014 3
2015 1
2016 1
2017 5
2018 3
2019 7
2020 6
2021 4
2022 2
2023 3

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128 results

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Page 1
Capillary Malformations.
Escobar K, Pandher K, Jahnke MN. Escobar K, et al. Dermatol Clin. 2022 Oct;40(4):425-433. doi: 10.1016/j.det.2022.06.005. Epub 2022 Sep 16. Dermatol Clin. 2022. PMID: 36243429 Review.
Most of the CMs occur without any syndromic findings; the association between CMs systemic anomalies in some patients, however, makes the recognition of additional syndrome features critical. Some genetic disorders discussed, which feature CMs, include Sturge-Weber
Most of the CMs occur without any syndromic findings; the association between CMs systemic anomalies in some patients, however, makes the re …
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 resul
Tongue Reduction for Macroglossia.
McCrossan S, Martin S, Hill C. McCrossan S, et al. J Craniofac Surg. 2021 Jul-Aug 01;32(5):1856-1859. doi: 10.1097/SCS.0000000000007276. J Craniofac Surg. 2021. PMID: 33235175 Review.
INTRODUCTION: Macroglossia is a term used to describe a large tongue which protrudes outside of the mouth while in a resting position (Balaji, 2013). It is a cardinal sign in children with Beckwith-Wiedemann syndrome and can also be found in children with Down syndrome
INTRODUCTION: Macroglossia is a term used to describe a large tongue which protrudes outside of the mouth while in a resting position (Balaj …
Orthopedic issues in vascular anomalies.
Spencer SA, Sorger JI. Spencer SA, et al. Semin Pediatr Surg. 2020 Oct;29(5):150973. doi: 10.1016/j.sempedsurg.2020.150973. Epub 2020 Sep 19. Semin Pediatr Surg. 2020. PMID: 33069292 Review.
For severe malformations, especially syndromes such as CLOVES and Klippel- Trenaunay syndrome, interdisciplinary team management is essential for the best outcomes....
For severe malformations, especially syndromes such as CLOVES and Klippel- Trenaunay syndrome, interdisciplinary team m …
Genetics of vascular anomalies.
Nguyen HL, Boon LM, Vikkula M. Nguyen HL, et al. Semin Pediatr Surg. 2020 Oct;29(5):150967. doi: 10.1016/j.sempedsurg.2020.150967. Epub 2020 Sep 16. Semin Pediatr Surg. 2020. PMID: 33069286 Review.
Vascular disorders.
Paller AS. Paller AS. Dermatol Clin. 1987 Jan;5(1):239-50. Dermatol Clin. 1987. PMID: 3030594 Review.
The most common associations are hypertrophy of underlying soft tissue and bone, as in the Klippel-Trenaunay-Weber and Sturge-Weber syndromes, visceral vascular lesions with hemorrhage, as in hereditary hemorrhagic telangiectasia and blue rubber bleb n …
The most common associations are hypertrophy of underlying soft tissue and bone, as in the Klippel-Trenaunay-Weber and …
Parkes Weber syndrome-Diagnostic and management paradigms: A systematic review.
Banzic I, Brankovic M, Maksimović Ž, Davidović L, Marković M, Rančić Z. Banzic I, et al. Phlebology. 2017 Jul;32(6):371-383. doi: 10.1177/0268355516664212. Epub 2016 Aug 9. Phlebology. 2017. PMID: 27511883 Review.
Although Parkes Weber syndrome is a clinically distinctive entity with serious complications, it is still frequently misdiagnosed as Klippel-Trenaunay syndrome that consists of the triad capillary malformation, venous malformation, and lymphatic …
Although Parkes Weber syndrome is a clinically distinctive entity with serious complications, it is still frequently misdiagno …
Imaging Findings of Klippel-Trenaunay Syndrome.
Abdel Razek AAK. Abdel Razek AAK. J Comput Assist Tomogr. 2019 Sep/Oct;43(5):786-792. doi: 10.1097/RCT.0000000000000895. J Comput Assist Tomogr. 2019. PMID: 31609295 Review.
We aim to review the imaging findings of Klippel-Trenaunay syndrome. This disorder characterized clinically by a triad of capillary malformations manifesting as a port-wine stain, venous varicosities typically along the lateral aspect of the lower extremities …
We aim to review the imaging findings of Klippel-Trenaunay syndrome. This disorder characterized clinically by a triad …
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 …
The Klippel-Trenaunay-Weber syndrome is characterized by the triad of a port-wine stain, varicose veins, and bon …
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 enlargeme …
Patients with Klippel-Trenaunay (KT) syndrome have a complex constellation of anomalies that includes cutaneous capilla …
128 results