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Neurogenetics. 2011 Aug;12(3):233-40. doi: 10.1007/s10048-011-0278-5. Epub 2011 Mar 2.

Familial spinal neurofibromatosis due to a multiexonic NF1 gene deletion.

Author information

1
Department of Experimental Medicine, Sapienza University, Rome, Italy.

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.

PMID:
21365283
DOI:
10.1007/s10048-011-0278-5
[Indexed for MEDLINE]

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