Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion

Antonio Pizzuti, Irene Bottillo, Francesca Inzana, Valentina Lanari, Francesca Buttarelli, Isabella Torrente, Anna Teresa Giallonardo, Alessandro De Luca, Bruno Dallapiccola

Research output: Contribution to journalArticle

Abstract

We report the detailed clinical presentation and molecular features of a spinal neurofibromatosis familial case where a 40-year-old woman, presenting with multiple bilateral spinal neurofibromas and no other clinical feature of neurofibromatosis type 1 (NF1), inherited a paternal large multiexonic deletion (c.5944-?-7126+?del) which resulted in NF1 gene haploinsufficiency at the RNA level. In the clinically unaffected 73-year-old father, spinal cord MRI disclosed bilateral and symmetrical hypertrophy of spinal lumbosacral roots. Our study widens the phenotypic and mutational spectrum of NF1 and illustrates the difficulties of counseling patients with border-line or atypical presentation of this disorder.

Original languageEnglish
Pages (from-to)233-240
Number of pages8
JournalNeurogenetics
Volume12
Issue number3
DOIs
Publication statusPublished - Aug 2011

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Keywords

  • FSNF
  • HSNF
  • Neurofibromatosis type 1
  • NF1
  • Spinal neurofibromas

ASJC Scopus subject areas

  • Genetics(clinical)
  • Cellular and Molecular Neuroscience
  • Genetics

Cite this

Pizzuti, A., Bottillo, I., Inzana, F., Lanari, V., Buttarelli, F., Torrente, I., Giallonardo, A. T., De Luca, A., & Dallapiccola, B. (2011). Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion. Neurogenetics, 12(3), 233-240. https://doi.org/10.1007/s10048-011-0278-5