Mandibular abnormalities in a patient with neurofibromatosis type 1.

Yeshwant B. Rawal, Molly S. Rosebush, Swati Y. Rawal, Kenneth Anderson

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder characterized by the presence of cutaneous neurofibromas, multiple cafd-au-lait spots and pigmented nodules of the iris known as Lisch nodules. In some cases, the diagnosis can be made at birth while in others the diagnosis is made later in life based on the appearance of additional criteria. We describe radiographic abnormalities of the mandible in a young adult male with NF1.

Original languageEnglish (US)
JournalThe Journal of the Tennessee Dental Association
Volume92
Issue number1
StatePublished - Jan 1 2012

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Neurofibromatosis 1
Neurofibromatoses
Iris
Mandible
Young Adult
Parturition
Skin

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Mandibular abnormalities in a patient with neurofibromatosis type 1. / Rawal, Yeshwant B.; Rosebush, Molly S.; Rawal, Swati Y.; Anderson, Kenneth.

In: The Journal of the Tennessee Dental Association, Vol. 92, No. 1, 01.01.2012.

Research output: Contribution to journalArticle

Rawal, Yeshwant B. ; Rosebush, Molly S. ; Rawal, Swati Y. ; Anderson, Kenneth. / Mandibular abnormalities in a patient with neurofibromatosis type 1. In: The Journal of the Tennessee Dental Association. 2012 ; Vol. 92, No. 1.
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