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dc.contributor.authorDİNÇER, Alp
dc.contributor.authorYapici, Zuhal
dc.contributor.authorObuz, Oguzhan
dc.contributor.authorYazici Gencdal, Isil
dc.date.accessioned2021-03-02T17:20:03Z
dc.date.available2021-03-02T17:20:03Z
dc.date.issued2020
dc.identifier.citationYazici Gencdal I., DİNÇER A., Obuz O., Yapici Z., "Leukoencephalopathy With Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL) A Case With Long-term Follow-up", NEUROLOGIST, cilt.25, ss.144-147, 2020
dc.identifier.issn1074-7931
dc.identifier.otherav_8c39d7bb-e759-44ea-99e2-b71bc06221f9
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/3693
dc.identifier.urihttps://doi.org/10.1097/nrl.0000000000000286
dc.description.abstractIntroduction: Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation (LBSL) is caused by a recessive mutation in the DARS2 gene and can be recognized by specific magnetic resonance imaging patterns. Case Report: A girl who developed leg tremors at age 4 years was diagnosed at age 17 years with LBSL -after evolution of ataxia and sensory loss. Examination at age 29 revealed mild spastic gait, ataxia, and sensory loss, and she did not require assistance to walk. Conclusion: This report illustrates the clinical and magnetic resonance imaging characteristics of a slowly progressive long-term course of childhood-onset LBSL.
dc.language.isoeng
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleLeukoencephalopathy With Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL) A Case With Long-term Follow-up
dc.typeMakale
dc.relation.journalNEUROLOGIST
dc.contributor.departmentBakirkoy Dr. Sadi Konuk Research & Training Hospital , ,
dc.identifier.volume25
dc.identifier.issue5
dc.identifier.startpage144
dc.identifier.endpage147
dc.contributor.firstauthorID2286575


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