Leigh hastalığı
Leigh hastalığı ya da juvenil subakut nekrotizan ensefalomyelopati, Leigh sendromu, infantil subakut nekrotizan ensefalomyelopati ve subakut nekrotizan ensefalomyelopati (SNEM),[1] merkezi sinir sistemini etkileyen nadir kalıtsal nörometabolik ve mitokondriyal bir hastalıktır. İngiliz nöropsikiyatrist Archibald Denis Leigh (1915-1998) tarafından ilk kez 1951 yılında tarif edilmiştir.[2]
Kaynakça
- ↑ "Leigh syndrome". Genetics Home Reference. National Institute of Health. 23 September 2013. 5 Eylül 2015 tarihinde kaynağından arşivlendi. http://web.archive.org/web/20150905130316/http://ghr.nlm.nih.gov/condition/leigh-syndrome. Erişim tarihi: 16 October 2013.
- ↑ "Obituaries". Psychiatric Bulletin 22 (10): 648. 1998. DOI:10.1192/pb.22.10.648. http://pb.rcpsych.org/cgi/reprint/22/10/648.pdf. Erişim tarihi: 16 October 2013.
Dış bağlantılar
- GeneReviews/NCBI/NIH/UW entry on Mitochondrial DNA-Associated Leigh Syndrome and NARP
- OMIM entries on Mitochondrial DNA-Associated Leigh Syndrome and NARP
- Leigh syndrome; Subacute necrotizing encephalopathy; Leigh's disease at NIH's Office of Rare Diseases
- leighsdisease at NINDS
- Maternally Inherited Leigh Syndrome at NIH's Office of Rare Diseases
- International Leigh syndrome community
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