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Neurofibromatosis type 1 x ray

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Moises Romo M.D.

Overview

There are no typical x-ray findings associated with neurofibromatosis type 1, however, X-rays may be helpful in the diagnosis of other complications such as scoliosis, slender long bones, skeletal dysplasia, tibial pseudoarthrosis, and osteoporosis.

X Ray

There are no x-ray findings associated with neurofibromatosis type 1.[1][2] However, an x-ray may be helpful in the diagnosis of complications of neurofibromatosis type 1, which include:

References

  1. 1.0 1.1 1.2 Gutmann DH, Ferner RE, Listernick RH, Korf BR, Wolters PL, Johnson KJ (February 2017). “Neurofibromatosis type 1”. Nat Rev Dis Primers. 3: 17004. doi:10.1038/nrdp.2017.4. PMID 28230061.
  2. 2.0 2.1 2.2 2.3 Invalid <ref> tag; no text was provided for refs named pmid26564071
  3. 3.0 3.1 3.2 “Neurofibromatosis Type 1 Workup: Laboratory Studies, Imaging Studies, Other Tests”.
  4. 4.0 4.1 4.2 Hirbe, Angela C; Gutmann, David H (2014). “Neurofibromatosis type 1: a multidisciplinary approach to care”. The Lancet Neurology. 13 (8): 834–843. doi:10.1016/S1474-4422(14)70063-8. ISSN 1474-4422.
  5. 5.0 5.1 “Neurofibromatosis type 1 | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”.
  6. Radtke HB, Sebold CD, Allison C, Haidle JL, Schneider G (August 2007). “Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors”. J Genet Couns. 16 (4): 387–407. doi:10.1007/s10897-007-9101-8. PMC 6338721. PMID 17636453.

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