| DC Field | Value | Language |
|---|
| 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 |
| Appears in Collections: | MedEspera 2018
|
