Klippel Trenaunay Syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-019-03178-x.pdf
Reference5 articles.
1. Wassef M, Blei F, Adams D, et al. Vascular anomalies classification: recommendations from the International Society for the Study of Vascular Anomalies. Pediatrics. 2015;136:e203.
2. Mulliken JB, Burrows PE, Fishman SJ. Mulliken and Young’s Vascular Anomalies: Hemangiomas and Malformations, 2nd ed. New York: Oxford University Press; 2013.
3. Luks VL, Kamitaki N, Vivero MP, et al. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. J Pediatr. 2015;166:1048–54.e1-5.
4. Brodkiewicz A, Szychot E, Peregud-Pogorzelski J, et al. Incomplete expression of Klippel–Trenaunay syndrome. Med Wieku Rozwoj. 2012;16:280–3.
5. Hammer J, Seront E, Duez S, et al. Sirolimus is efficacious in treatment for extensive and/or complex slow-flow vascular malformations: a monocentric prospective phase II study. Orphanet J Rare Dis. 2018;13:191.
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1. A rare case of Klippel–Trenaunay syndrome in a neonate;Karnataka Paediatric Journal;2023-12-09
2. Subcutaneous Cavernous Haemangioma in a Patient with Klippel-Trenaunay Syndrome: A Case Report;Current Medical Imaging Reviews;2023-11-28
3. SÍNDROME DE KLIPPEL – TRENAUNAY: RELATO DE CASO CLÍNICO UNUSUAL COM ACOMPANHAMENTO DE 11 ANOS;Revista Contemporânea;2023-08-24
4. Easily misdiagnosed complex Klippel-Trenaunay syndrome: A case report;World Journal of Clinical Cases;2023-02-06
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