A novel mutation in the FOXC2 gene: a heterozygous insertion of adenosine (c.867insA) in a family with lymphoedema of lower limbs without distichiasis
Author:
Affiliation:
1. Dermatovenereological Clinic , University Medical Centre Ljubljana , Ljubljana , Slovenia
2. Faculty of Medicine, University of Maribor , Maribor , Slovenia
3. University Clinic of Respiratory and Allergic Diseases Golnik , Golnik , Slovenia
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Radiology, Nuclear Medicine and imaging,Oncology
Reference35 articles.
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2. Smeltzer DM, Stickler GB, Schirger A. Primary lymphedema in children and adolescents: a follow-up study and review. Pediatrics 1985: 76: 206-18.
3. Al-Niaimi F, Cox N. Cellulitis in lymphoedema: a vicious cycle. J Lymph 2009; 42: 38-42.
4. Sharma A, Schwartz RA. Stewart-Treves syndrome: pathogenesis and management. J Am Acad Dermatol 2012; 67:1342-8. 10.1016/j.jaad.2012.04.028
5. Dürr HR, Pellengahr C, Nerlich A, Baur A, Maier M, Jansson V. Stewart-Treves syndrome as a rare complication of a hereditary lymphedema. Vasa 2004; 33: 42-5. 10.1024/0301-1526.33.S65.42
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