Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report

Neurofibromatosis Type I (NFI) is a relatively common hereditary, autosomal dominant neurocutaneous condition. It is a benign peripheral nerve sheath tumour arising from Schwann cells and peripheral fibroblasts. Even though it is a neurocutaneous disorder, NF I has significant skeletal manifestati...

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Main Authors: Bhuvana Krishnamoorthy, Parul Singh, Suma Gundareddy N, Manisha Lakhanpal Sharma, Manu Dhillon
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2013-10-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/3534/90-%205952_E(C)_F(P)_PF1(HM).pdf
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spelling doaj-9f239e0c01d845358b949dbc9e9d377b2020-11-25T01:55:22ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2013-10-017102390239110.7860/JCDR/2013/5952.3534Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case ReportBhuvana Krishnamoorthy0Parul Singh1Suma Gundareddy N2Manisha Lakhanpal Sharma3Manu Dhillon4Associate Professor, Department of Oral Medicine and Radiology, ITS- Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP, India. Post Graduate Student, Department of Oral Medicine and Radiology, ITS- Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP, India. Professor and Head, Department of Oral Medicine and Radiology, ITS- Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP, India. Reader, Department of Oral Medicine and Radiology, ITS- Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP, India.Senior Lecturer, Department of Oral Medicine and Radiology, ITS- Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP, India. Neurofibromatosis Type I (NFI) is a relatively common hereditary, autosomal dominant neurocutaneous condition. It is a benign peripheral nerve sheath tumour arising from Schwann cells and peripheral fibroblasts. Even though it is a neurocutaneous disorder, NF I has significant skeletal manifestations. Oral and maxillofacial skeletal structures are also often involved in the form of deepening of sigmoid notch, enlarged mandibular canal and notching of inferior border of mandible. In this paper, we are reporting a female patient of NF I who presented with a notching in the posterior border of ascending ramus of mandible.https://jcdr.net/articles/PDF/3534/90-%205952_E(C)_F(P)_PF1(HM).pdfneurofibromatosis type imandibleneurofibromin
collection DOAJ
language English
format Article
sources DOAJ
author Bhuvana Krishnamoorthy
Parul Singh
Suma Gundareddy N
Manisha Lakhanpal Sharma
Manu Dhillon
spellingShingle Bhuvana Krishnamoorthy
Parul Singh
Suma Gundareddy N
Manisha Lakhanpal Sharma
Manu Dhillon
Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
Journal of Clinical and Diagnostic Research
neurofibromatosis type i
mandible
neurofibromin
author_facet Bhuvana Krishnamoorthy
Parul Singh
Suma Gundareddy N
Manisha Lakhanpal Sharma
Manu Dhillon
author_sort Bhuvana Krishnamoorthy
title Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
title_short Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
title_full Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
title_fullStr Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
title_full_unstemmed Notching in the Posterior Border of the Ramus of Mandible in a Patient with Neurofibromatosis Type I – A Case Report
title_sort notching in the posterior border of the ramus of mandible in a patient with neurofibromatosis type i – a case report
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2013-10-01
description Neurofibromatosis Type I (NFI) is a relatively common hereditary, autosomal dominant neurocutaneous condition. It is a benign peripheral nerve sheath tumour arising from Schwann cells and peripheral fibroblasts. Even though it is a neurocutaneous disorder, NF I has significant skeletal manifestations. Oral and maxillofacial skeletal structures are also often involved in the form of deepening of sigmoid notch, enlarged mandibular canal and notching of inferior border of mandible. In this paper, we are reporting a female patient of NF I who presented with a notching in the posterior border of ascending ramus of mandible.
topic neurofibromatosis type i
mandible
neurofibromin
url https://jcdr.net/articles/PDF/3534/90-%205952_E(C)_F(P)_PF1(HM).pdf
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