Generalized metabolic bone disease in Neurofibromatosis type I
✍ Scribed by Nicola Brunetti-Pierri; Stephen B. Doty; John Hicks; Kelly Phan; Roberto Mendoza-Londono; Maria Blazo; Alyssa Tran; Susan Carter; Richard Alan Lewis; Sharon E. Plon; William A. Phillips; E. O’Brian Smith; Kenneth J. Ellis; Brendan Lee
- Book ID
- 116988326
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 1017 KB
- Volume
- 94
- Category
- Article
- ISSN
- 1096-7192
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Neurofibromatosis type 1 (NF1), or von Recklinghausen disease is a genetic disease characterized by a variety of multiple clinical symptoms affecting primarily cells of neural crest origin, and is therefore classified as neurocristopathy. The most clinically significant feature of the disease is the
Objectives/Hypothesis: To describe the histopathologic findings in the temporal bone in patients with neurofibromatosis type 2 (NF2). The literature contains limited data on otopathology of NF2. Study Design: Basic science study. Methods: Twenty-six temporal bones from 16 patients with NF2 were exa