When Neurofibromatosis Meets Diabetes: A Long-Term Follow-up in a Pediatric Case Report
Author:
Funder
novo nordisk
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s42399-023-01402-6.pdf
Reference39 articles.
1. Evans DG, Howard E, Giblin C, Clancy T, Spencer H, Huson SM, et al. Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service. Am J Med Genet Part A. 2010;152:327–32.
2. Neurofibromatosis. Conference statement. National institutes of health consensus development conference. Arch Neurol. 1988;45(5):575–8.
3. Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, et al. Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation. Genet Med. 2021;23(8):1506–13. https://doi.org/10.1038/s41436-021-01170-5.
4. Jett K, Friedman JM. Clinical and genetic aspects of neurofibromatosis 1. Genet Med. 2010;12:1–11.
5. Ozhan B, Ozguven AA, Ersoy B. Neurofibromatosis type 1 and diabetes mellitus: an unusual association. Case Rep Endocrinol. 2013;2013:689107. https://doi.org/10.1155/2013/689107.
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