Co-occurrence of Sturge-Weber syndrome phenotype and Klippel-Trenaunay-Weber syndrome phenotype in a patient: Molecular evidence of the shared pathological basis of the two conditions

SAKAGUCHI Yuri; TAKENOUCHI Toshiki; TAKENOUCHI Toshiki; TAKAHASHI Takao; KOSAKI Kenjiro

Art

J-GLOBAL ID：201702254423990082 Reference number：17A0285674

Co-occurrence of Sturge-Weber syndrome phenotype and Klippel-Trenaunay-Weber syndrome phenotype in a patient: Molecular evidence of the shared pathological basis of the two conditions

患者におけるSturge-Weber症候群表現型およびKlippel-Trenaunay-Weber症候群表現型の同時発生 2つの条件の共有された病理学基盤の分子的証明

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Material：
Volume： 61st(Web) Page： ROMBUNNO.Thu(5)-O43-2 (WEB ONLY) Publication year： 2016
JST Material Number： L1204A Document type： Proceedings
Article type：短報 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Congenital diseases,deformities in general. , Tumors(=neoplasms)of cardiovascular system , Nervous system diseases

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