| A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma. | |
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MedLine Citation:
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PMID: 15356469 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Neurofibromatosis Type 1 (NF1) is one of the most common autosomal dominant diseases affecting multiple systems including the vascular, skeletal, and central nervous system. Noonan syndrome (NS) is an autosomal dominant genetic disorder, associated with musculoskeletal and skin manifestations. Coexistence of central giant cell lesions in patients with both NS and NF1 were reported in the literature. Development of multiple central giant cell lesions in a patient with a Noonan syndrome has been referred to as Noonan-like syndrome. A few cases with features of NF1 and NS have been termed as NF1-NS. Here, we present a case of so-called NF-NS associated with a central giant cell lesion. |
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Authors:
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Maryam Yazdizadeh; Jose Luis Tapia; Maryam Baharvand; Lida Radfar |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics Volume: 98 ISSN: 1079-2104 ISO Abbreviation: Oral Surg Oral Med Oral Pathol Oral Radiol Endod Publication Date: 2004 Sep |
Date Detail:
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Created Date: 2004-09-09 Completed Date: 2004-11-09 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 9508562 Medline TA: Oral Surg Oral Med Oral Pathol Oral Radiol Endod Country: United States |
Other Details:
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Languages: eng Pagination: 316-20 Citation Subset: D; IM |
Affiliation:
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School of Dentistry, University of Shaheed Beheshti, Tehran, Iran. |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Adult Granuloma, Giant Cell / complications* Humans Male Maxillary Diseases / complications* Mental Retardation / complications Neurofibromatosis 1 / complications* Noonan Syndrome / complications* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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