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Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_52350ef3ec5a426384f6f30cd01656d8

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

About this item

Full title

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Publisher

Cairo, Egypt: Hindawi Publishing Corporation

Journal title

Case reports in orthopedics, 2018, Vol.2018 (2018), p.1-5

Language

English

Formats

Publication information

Publisher

Cairo, Egypt: Hindawi Publishing Corporation

More information

Scope and Contents

Contents

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...

Alternative Titles

Full title

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_52350ef3ec5a426384f6f30cd01656d8

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_52350ef3ec5a426384f6f30cd01656d8

Other Identifiers

ISSN

2090-6749

E-ISSN

2090-6757

DOI

10.1155/2018/7698052

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