Foster Kennedy syndrome as an initial presentation of neurofibromatosis type 2: a case report

dc.contributor.author	Sumleanschi, Alexandru
dc.contributor.author	Borodin, Serghei
dc.date.accessioned	2020-07-02T14:40:18Z
dc.date.available	2020-07-02T14:40:18Z
dc.date.issued	2018
dc.identifier.citation	SUMLEANSCHI, Alexandru, BORODIN, Serghei. Foster Kennedy syndrome as an initial presentation of neurofibromatosis type 2: a case report. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 28-29.	en_US
dc.identifier.uri	https://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf
dc.identifier.uri	http://repository.usmf.md/handle/20.500.12710/10856
dc.description	Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova	en_US
dc.description.abstract	Background. Foster Kennedy syndrome (FKS) is described as ipsilateral optic atrophy and contralateral papilledema from an intracranial mass. FKS is uncommon manifestation of Neurofibromatosis type 2 (NF2), which is generally presented with hearing loss and tinnitus.	en_US
dc.language.iso	en	en_US
dc.publisher	MedEspera	en_US
dc.subject	Foster Kennedy syndrome	en_US
dc.subject	neurofibromatosis type 2	en_US
dc.subject	intracranial meningioma	en_US
dc.subject	intramedullary tumor	en_US
dc.subject	extramedullary tumor	en_US
dc.title	Foster Kennedy syndrome as an initial presentation of neurofibromatosis type 2: a case report	en_US
dc.type	Article	en_US