1. Further case of enlarged spinal nerve roots in KRAS-related Noonan syndrome.
- Author
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Leoni C, Viscogliosi G, Onesimo R, Verdolotti T, Biagini T, Mazza T, De Luca A, Perri L, Trevisan V, Flex E, Tartaglia M, and Zampino G
- Subjects
- Humans, Proto-Oncogene Proteins p21(ras) genetics, Spinal Nerve Roots diagnostic imaging, Mutation, Noonan Syndrome diagnosis, Noonan Syndrome genetics, Neurofibromatosis 1 complications, Neurofibromatosis 1 diagnosis, Neurofibromatosis 1 genetics, Neurofibromatoses
- Abstract
Noonan syndrome (NS) belongs to RASopathies, a family of disorders caused by unregulated signaling through the RAS-MAPK pathway. Herein, we report on an individual with molecularly confirmed diagnosis of NS showing asymptomatic enlarged spinal nerve roots, which are distinctive features of neurofibromatosis type 1. To date, a total of 16 patients with neurogenic tumors resembling neurofibromas/schwannomas and a molecularly confirmed diagnosis of a non-NF1 RASopathy have been reported, adding this further feature shared among RASopathies., (© 2023 The Authors. Clinical Genetics published by John Wiley & Sons Ltd.)
- Published
- 2023
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