Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome
Joint Authors
Lysy, Philippe A.
Miri, Othmane
Bonnet, Nicolas
Loucheur, Naima
Gayito, René
Docquier, Pierre-Louis
Source
Issue
Vol. 2018, Issue 2018 (31 Dec. 2018), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2018-12-06
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
Noonan-like/multiple giant cell lesion (NS/MGCL) is a rare condition overlapping with Noonan syndrome.
Once thought to be a specific and separate entity, it is now suggested to be a variant of the Noonan syndrome spectrum.
We report the case of an 8-year-old boy with a typical clinical picture of Noonan syndrome with a de novo germline mutation of PTPN11 (c.854 T>C).
During his follow-up, the patient developed multifocal pigmented villonodular synovitis which first affected the left knee and shortly after both elbows.
American Psychological Association (APA)
Miri, Othmane& Bonnet, Nicolas& Lysy, Philippe A.& Loucheur, Naima& Gayito, René& Docquier, Pierre-Louis. 2018. Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome. Case Reports in Orthopedics،Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1147916
Modern Language Association (MLA)
Miri, Othmane…[et al.]. Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome. Case Reports in Orthopedics No. 2018 (2018), pp.1-5.
https://search.emarefa.net/detail/BIM-1147916
American Medical Association (AMA)
Miri, Othmane& Bonnet, Nicolas& Lysy, Philippe A.& Loucheur, Naima& Gayito, René& Docquier, Pierre-Louis. Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome. Case Reports in Orthopedics. 2018. Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1147916
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1147916
