dc.creatorBarrientos, Laura Soledad
dc.creatorMaiolini, Arianna
dc.creatorHäni, Anna Katrin
dc.creatorJagannathan, Vidya
dc.creatorLeeb, Tosso
dc.date2018-12-07
dc.date2021-09-23T17:50:59Z
dc.date.accessioned2023-07-15T03:09:24Z
dc.date.available2023-07-15T03:09:24Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/125525
dc.identifierissn:1365-2052
dc.identifierissn:0268-9146
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7464651
dc.descriptionLafora disease is an autosomal recessive disorder that causes myoclonic epilepsy1,2,3. The disease is characterized by the presence of polyglucosan inclusion bodies (Lafora bodies), predominantly in the central nervous system. More than 90% of human Lafora disease cases are caused by genetics variants in either EPM2A, encoding the laforin glucan phosphatase or NHLRC1 encoding the NHL repeat containing E3 ubiquitin protein ligase 1, which has also been termed EPM2B or malin1,2,4 . Lafora disease in animals has similar clinical signs as the human disease, including spontaneous and reflex myoclonus, jerks and generalized tonic clonic seizures. Case description: A 10-year old female spayed Chihuahua was presented at the Small Animal Hospital of the University of Bern. Lafora disease was suspected based on neurological examination, seizures semiology, MRI and CSF findings. An EDTA blood sample was collected for further genetic analysis.
dc.descriptionInstituto de Genética Veterinaria
dc.formatapplication/pdf
dc.format118-119
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.subjectCiencias Veterinarias
dc.subjectTrinucleotide repeat expansion
dc.subjectWhole genome sequencing
dc.subjectLafora disease
dc.subjectDna repeat expansion
dc.subjectGenetic variants
dc.subjectGenetics
dc.subjectBiology
dc.titleNHLRC1 dodecamer repeat expansion demonstrated by whole genome sequencing in a Chihuahua with Lafora disease
dc.typeArticulo
dc.typeComunicacion


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