Here we describe a case of Neurofibromatosis type 1 (NF1) associated with an atypical histiocytic lesion and a new pathogenic mutation. The genetic analysis revealed an heterozygous mutation in the 5' splice site of intron 32, 6,084 + 1G -> T. Histopathological findings are compatible with juvenile xanthogranuloma. The new, not already described, splicing mutation, is possibly partly responsible of the association between NF1 and the histiocitic lesion.

An histologically atypical NF-type 1 patient with a new pathogenic mutation / Giovanni, Bianco; Giuseppe, Greco; Antonelli, Manila; Stefania, Casali; Cinzia, Castagnini. - In: NEUROLOGICAL SCIENCES. - ISSN 1590-1874. - ELETTRONICO. - 33:6(2012), pp. 1483-1485. [10.1007/s10072-011-0897-5]

An histologically atypical NF-type 1 patient with a new pathogenic mutation

ANTONELLI, MANILA;
2012

Abstract

Here we describe a case of Neurofibromatosis type 1 (NF1) associated with an atypical histiocytic lesion and a new pathogenic mutation. The genetic analysis revealed an heterozygous mutation in the 5' splice site of intron 32, 6,084 + 1G -> T. Histopathological findings are compatible with juvenile xanthogranuloma. The new, not already described, splicing mutation, is possibly partly responsible of the association between NF1 and the histiocitic lesion.
2012
heterozygous mutation; neurofibromatosis type 1; gene analysis; juvenile xanthogranuloma; atypical histiocytic lesion; von recklinghausen disease; neurofibromatosis; juvenile; anthogranuloma
01 Pubblicazione su rivista::01a Articolo in rivista
An histologically atypical NF-type 1 patient with a new pathogenic mutation / Giovanni, Bianco; Giuseppe, Greco; Antonelli, Manila; Stefania, Casali; Cinzia, Castagnini. - In: NEUROLOGICAL SCIENCES. - ISSN 1590-1874. - ELETTRONICO. - 33:6(2012), pp. 1483-1485. [10.1007/s10072-011-0897-5]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/650085
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