Neurofibromatosis type 1 with unusual oral manifestations

Neurofibromatosis (NF) is a genetically transmitted autosomal dominant disorder with variable penetrance and about 50% of cases representing new mutations. It is progressive in nature and one of its unique feature is the diversity of clinical expression from one patent to another and even within a f...

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Main Authors: Raghavendra Kini (Author), Vathsala Naik (Author), Ashwini Baliga (Author), Anjali P Shetty (Author), Y R Girish (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2012-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Raghavendra Kini  |e author 
700 1 0 |a Vathsala Naik  |e author 
700 1 0 |a Ashwini Baliga  |e author 
700 1 0 |a Anjali P Shetty  |e author 
700 1 0 |a Y R Girish  |e author 
245 0 0 |a Neurofibromatosis type 1 with unusual oral manifestations 
260 |b Wolters Kluwer Medknow Publications,   |c 2012-01-01T00:00:00Z. 
500 |a 0972-1363 
500 |a 0975-1572 
520 |a Neurofibromatosis (NF) is a genetically transmitted autosomal dominant disorder with variable penetrance and about 50% of cases representing new mutations. It is progressive in nature and one of its unique feature is the diversity of clinical expression from one patent to another and even within a family. The disease is often characterized by complex and multicellular neurofibroma. It may also lead to different complications throughout the life of an affected individual. We report a case of NF involving alveolus of maxilla and mandible causing expansion of the buccal and lingual cortical plates in a 10-year-old girl 
546 |a EN 
690 |a Neurofibromatosis 
690 |a Mandible 
690 |a Hypoplastic 
690 |a Café au lait spots 
690 |a Dentistry 
690 |a RK1-715 
690 |a Medical physics. Medical radiology. Nuclear medicine 
690 |a R895-920 
655 7 |a article  |2 local 
786 0 |n Journal of Indian Academy of Oral Medicine and Radiology, Vol 24, Iss 3, Pp 226-229 (2012) 
787 0 |n http://www.jiaomr.in/article.asp?issn=0972-1363;year=2012;volume=24;issue=3;spage=226;epage=229;aulast=Kini 
787 0 |n https://doaj.org/toc/0972-1363 
787 0 |n https://doaj.org/toc/0975-1572 
856 4 1 |u https://doaj.org/article/8b8d239fe91a43b0a1f48d18949f28d1  |z Connect to this object online.