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Loss of Heterozygosity of the APC Gene in a Case of Vestibular Schwannoma Assessed by Two Intragenetic Markers

Nives Pećina-Šlaus orcid id orcid.org/0000-0002-3334-7671


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Abstract

Schwannomas are benign encapsulated tumors of Schwann cells, the main peripheral glia cells. The majority of schwannomas arise spontaneously and account for 8% of intracranial tumors. Those involving the cerebellopontine angle are schwannomas in 90% of cases. A case is presented of the loss of heterozygosity of the adenomatous polyposis coli (APC) gene in a female patient with cranial schwannoma from Croatia. The observed change of the APC gene was investigated by use of two intragenetic markers. In the light of novel findings on merlin connection to the wnt signaling reported in the literature, the finding of gross deletion in a patient with cranial vestibular schwannoma is a relevant genetic event.

Keywords

Schwannoma; APC gene; Loss of heterozygosity; Neurinoma

Hrčak ID:

107965

URI

https://hrcak.srce.hr/107965

Publication date:

1.12.2012.

Article data in other languages: croatian

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