Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/51380
Title: Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation
Authors: Piranit Nik Kantaputra
Ans van den Ouweland
Tumtip Sangruchi
Chanin Limwongse
Keywords: Biochemistry, Genetics and Molecular Biology
Medicine
Issue Date: 1-Jul-2012
Abstract: A Thai woman, who was affected with neurofibromatosis type 1, was followed up and re-evaluated at ages 45, 61, and 67 years. Her mother and her three brothers were also affected. The proposita was very severely affected. She was born blind with underdeveloped eyeglobes and had large plexiform neurofibromas on her face. Her eyelids were gigantic and tears drained from the orifice between them. Cutaneous neurofibromas were observed all over her body. A novel mutation c.4821delA was identified in NF1 gene, which predicted truncation of neurofibromin (p.Leu1607fs). © 2012 Wiley Periodicals, Inc.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862704574&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/51380
ISSN: 15524833
15524825
Appears in Collections:CMUL: Journal Articles

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