Document Detail


A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
MedLine Citation:
PMID:  15356469     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Maryam Yazdizadeh; Jose Luis Tapia; Maryam Baharvand; Lida Radfar
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
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:
Created Date:  2004-09-09     Completed Date:  2004-11-09     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9508562     Medline TA:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod     Country:  United States    
Other Details:
Languages:  eng     Pagination:  316-20     Citation Subset:  D; IM    
Affiliation:
School of Dentistry, University of Shaheed Beheshti, Tehran, Iran.
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MeSH Terms
Descriptor/Qualifier:
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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