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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Format: | Book |
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Wolters Kluwer Medknow Publications,
2012-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_8b8d239fe91a43b0a1f48d18949f28d1 | ||
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. |