Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines

Erin Conboy, Radhika Dhamija, Margaret Wang, Jing Xie, Peter J Dyck, Alina G. Bridges, Robert J. Spinner, Amy C. Clayton, Robert E. Watson, Ludwine Messiaen, Dusica Babovic-Vuksanovic

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

Background Noonan syndrome with multiple lentigines (NSML), formerly known as LEOPARD syndrome, is an autosomal-dominant disorder characterised by lentigines, EKG abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, growth retardation and deafness. There is significant clinical overlap between NSML and other disorders that result from dysregulated rat sarcoma/mitogen-activated protein kinase pathway (RASopathies). Except for neurofibromatosis type 1, other RASopathies are not known to be typically associated with neurogenic tumours. Methods and results We evaluated patients from three families with pigmentary skin lesions, progressive neuropathy, enlarged nerves, massive burden of paraspinal tumours (neurofibroma was confirmed in one patient) and a clinical diagnosis of NSML. All patients had a mutation in the protein tyrosine phosphatase catalytic domain of the PTPN11 gene; two unrelated patients had the p.Thr468Met mutation, while the family consisting of two affected individuals harboured the p.Thr279Cys mutation. Molecular analysis performed on hypertrophic nerve tissue did not disclose a second somatic hit in NF1, PTPN11, NF2 or SMARCB1 genes. Conclusions Neurogenic tumours and hypertrophic neuropathy are unusual complications of NSML and may be an under-recognised manifestation that would warrant surveillance. Our observation may also have implications for other disorders caused by RAS-pathway dysregulation.

Original languageEnglish (US)
Pages (from-to)123-126
Number of pages4
JournalJournal of Medical Genetics
Volume53
Issue number2
DOIs
StatePublished - Sep 2 2015

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Conboy, E., Dhamija, R., Wang, M., Xie, J., Dyck, P. J., Bridges, A. G., Spinner, R. J., Clayton, A. C., Watson, R. E., Messiaen, L., & Babovic-Vuksanovic, D. (2015). Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines. Journal of Medical Genetics, 53(2), 123-126. https://doi.org/10.1136/jmedgenet-2015-103177