c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and robin sequence in a Thai patient

• Main Authors: Tanpaiboon,P., Kantaputra,P.N.I., Wejathikul,K., Piyamongkol,W.
• Format: Article
• Published: Wiley-Liss Inc. 2015
• Subjects: Genetics (clinical); Genetics
• Online Access: http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77649227668&origin=inward; http://cmuir.cmu.ac.th/handle/6653943832/38173
• Institution: Chiang Mai University

Lymphedema - distichiasis syndrome is a rare primary lymphedema inherited as an autosomal dominant disorder. The characteristic features consist of late onset-lymphedema and distichiasis together with other occasionally seen features including varicose vein, cleft palate, ptosis, and congenital hear...