
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Neurofibromatosis type 1 x ray
Introduction
Overview
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
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:
- Scoliosis. Measure Cobb angle.[3][1][2]
- Pseudarthrosis[4]
- Chest-wall deformity[4]
- Long bone bowing and obliteration of the intramedullary spaces.[3][1][2]
- Bone dysplasias[4]
- Presence of osteophytes.[3][2]
- Kyphosis_Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program-5|[5]
- Spina bifida _Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program-5|[5] [6]
References
References
- ↑ 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.
- ↑ 2.0 2.1 2.2 2.3 Invalid
<ref>tag; no text was provided for refs namedpmid26564071 - ↑ 3.0 3.1 3.2 “Neurofibromatosis Type 1 Workup: Laboratory Studies, Imaging Studies, Other Tests”.
- ↑ 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.
- ↑ _Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program_5-0|5.0 _Genetic_and_Rare_Diseases_Information_Center_(GARD)_–_an_NCATS_Program_5-1|5.1 “Neurofibromatosis type 1 | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”.
- ↑ 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.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Moises Romo M.D.
