Late onset presentation of Leigh syndrome on two cases
Author:
Affiliation:
1. Federal Fluminense University; Federal Fluminense University, Brazil
2. Federal Fluminense University, Brazil; Federal Fluminense University, Brazil
3. UFF; UNIGRANRIO
Publisher
FapUNIFESP (SciELO)
Subject
Neurology,Neurology (clinical)
Link
http://www.scielo.br/pdf/anp/v68n3/v68n3a27.pdf
Reference10 articles.
1. Uma revisão clínico-laboratorial da síndrome de Leigh baseada em 7 casos;Fernandes AR
2. Atypical presentations of Leigh syndrome: a case series and review;Huntsman RJ;Pediatr Neurol,2005
3. Progressive dystonia with bilateral putaminal hypodensities;Berkovic SF;Arch Neurol,1987
4. Mechanisms of unexpected death and autopsy findings in Leigh syndrome (subacute necrotising encephalomyelopathy);Wick R;J Forensic Leg Med,2007
5. Diagnosis and management of mitochondrial respiratory chain disorders;Bhattacharya K;Curr Paediatr,2003
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1. Reply to the letter: “Is the variant m.9176T>C in MT‐ATP6 truly responsibly for Leigh syndrome?”;Pediatrics International;2021-02
2. Adult Presentation of Subacute Necrotizing Encephalomyelopathy in Two Siblings;Cureus;2019-08-29
3. A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications;Mitochondrion;2019-05
4. Late-onset Leigh syndrome due to NDUFV1 mutation in a 10-year-old boy initially presenting with ataxia;Journal of Pediatric Neurosciences;2018
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