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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 manifestation...

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Autori principali: Krishnamoorthy, Bhuvana, Singh, Parul, Gundareddy, Suma N, Sharma, Manisha Lakhanpal, Dhillon, Manu
Natura: Artigo
Lingua:Inglês
Pubblicazione: JCDR Research and Publications (P) Limited 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3843395/
https://ncbi.nlm.nih.gov/pubmed/24298539
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2013/5952.3534
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