Publication:
Madras motor neuron disease in Turkey

dc.contributor.authorİŞAK, BARIŞ
dc.contributor.authorsIsak, Baris; Uluc, Kayihan; Tanridag, Tulin; Ozsahin, Selda; Dengler, Reinhard; Us, Onder; Petri, Susanne
dc.date.accessioned2022-03-12T17:37:52Z
dc.date.available2022-03-12T17:37:52Z
dc.date.issued2009
dc.description.abstractWe present a 19-year-old female patient complaining of hoarseness and eyelid drooping. The neurological examination and laboratory investigations including genetic, radiological and electrophysiological evaluations were consistent with a juvenile-onset, predominantly bulbar, motor neuron disease with sensorineural hearing loss. The syndrome fulfilled the diagnostic criteria of Madras Motor Neuron Disease (MMND). Very few cases with MMND have been reported to date, and the majority are from south-eastern Asia. This is the first case reported from Turkey and indicates that the disease is not only regional but may also occur on the basis of rare de novo mutations.
dc.identifier.doi10.3109/17482960802645016
dc.identifier.eissn1471-180X
dc.identifier.issn1748-2968
dc.identifier.pubmed19922122
dc.identifier.urihttps://hdl.handle.net/11424/229425
dc.identifier.wosWOS:000272294000012
dc.language.isoeng
dc.publisherINFORMA HEALTHCARE
dc.relation.ispartofAMYOTROPHIC LATERAL SCLEROSIS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMotor neuron disease
dc.subjectMadras motor neuron disease
dc.subjectbulbar onset
dc.subjectPATTERN
dc.titleMadras motor neuron disease in Turkey
dc.typearticle
dspace.entity.typePublication
local.avesis.id0f90313a-6df7-4f18-81dd-5a79c048d5c7
local.import.packageSS17
local.indexed.atWOS
local.indexed.atSCOPUS
local.indexed.atPUBMED
local.journal.numberofpages3
oaire.citation.endPage349
oaire.citation.issue5-6
oaire.citation.startPage347
oaire.citation.titleAMYOTROPHIC LATERAL SCLEROSIS
oaire.citation.volume10
relation.isAuthorOfPublication3978eebd-304b-4af3-930c-2db9759c860d
relation.isAuthorOfPublication.latestForDiscovery3978eebd-304b-4af3-930c-2db9759c860d

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