| Literature DB >> 33676063 |
Chiara Leoni1, Marta Tedesco2, Dario Talloa2, Tommaso Verdolotti3, Roberta Onesimo2, Cesare Colosimo4, Elisabetta Flex5, Alessandro De Luca6, Marco Tartaglia7, Donato Rigante8, Giuseppe Zampino8.
Abstract
RASopathies are a group of genetic conditions caused by germline variants in genes encoding signal transducers and modulators of the RAS-MAPK cascade. These disorders are multisystem diseases with considerable clinical overlap, even though distinct hallmarks are recognizable for each specific syndrome. Here we report on the presence of enlarged spinal nerve roots resembling neurofibromas, a typical neuroradiological finding of neurofibromatosis type 1, in two patients with a molecularly confirmed diagnosis of Noonan syndrome and cardio-facio-cutaneous syndrome, respectively. This evidence add enlarged spinal nerve roots as features shared among RASopathies. Future studies aiming to a better understanding of the molecular mechanisms leading to neurogenic tumor development in these patients are necessary to define their biological nature, evolution, prognosis and possible treatments.Entities:
Keywords: Cardio-facio-cutaneous syndrome; Diagnostic accuracy; Noonan syndrome; RASopathies; Tailored treatments
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Year: 2021 PMID: 33676063 DOI: 10.1016/j.ejmg.2021.104187
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.465