Literature DB >> 15866434

Atypical presentations of leigh syndrome: a case series and review.

Richard J Huntsman1, D Barry Sinclair, Ravi Bhargava, Alicia Chan.   

Abstract

Patients with Leigh syndrome classically present in early childhood with developmental regression, ataxia, and hypotonia with subsequent respiratory and brainstem dysfunction. However, the clinical presentation can be highly variable. This report presents five cases of Leigh syndrome with atypical presentations. The first patient is a 17-month-old female who presented with progressive limb weakness diagnosed as Guillain-Barre syndrome. Postmortem examination demonstrated Leigh syndrome confined to the spinal cord. The case series then describes two sisters one of whom presented at 11 years of age with central respiratory failure and encephalopathy. Her 15-year-old sister presented with a progressive diplegia. The fourth patient presented with bronchiolitis and apnea at 3 months of age due to bilateral brainstem lesions. Her second cousin presented at 6 months of age with hypotonia, blindness, and tonic seizures. All patients had laboratory and radiologic findings consistent with Leigh syndrome. Evidence of spinal cord involvement was observed on magnetic resonance imaging in four of the five patients. Leigh syndrome can involve any level of the neuroaxis, resulting in a wide variety of presentations. Many atypical variants are observed, of which clinicians should be aware. Evidence of brainstem or spinal cord involvement should also be sought in patients with Leigh syndrome.

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Year:  2005        PMID: 15866434     DOI: 10.1016/j.pediatrneurol.2004.12.009

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  11 in total

1.  Genetic and clinical features of Chinese patients with mitochondrial ataxia identified by targeted next-generation sequencing.

Authors:  Hai-Lin Dong; Yin Ma; Quan-Fu Li; Yi-Chu Du; Lu Yang; Sheng Chen; Zhi-Ying Wu
Journal:  CNS Neurosci Ther       Date:  2018-05-13       Impact factor: 5.243

2.  Leigh's Disease: The Acute Clinical Course of a Two-Year-Old Child with Subacute Necrotizing Encephalomyelopathy.

Authors:  Bettina Zinka; Andreas Buettner; Matthias Graw
Journal:  Case Rep Med       Date:  2010-06-10

3.  Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).

Authors:  Shanti Balasubramaniam; B Lewis; D M Mock; H M Said; M Tarailo-Graovac; A Mattman; C D van Karnebeek; D R Thorburn; R J Rodenburg; J Christodoulou
Journal:  JIMD Rep       Date:  2016-07-22

4.  TMEM65 is a mitochondrial inner-membrane protein.

Authors:  Naotaka Nishimura; Tomomi Gotoh; Yuichi Oike; Masato Yano
Journal:  PeerJ       Date:  2014-04-10       Impact factor: 2.984

5.  Spinal cord involvement in Kearns-Sayre syndrome: a neuroimaging study.

Authors:  Pasquini Luca; Guarnera Alessia; Rossi-Espagnet Maria Camilla; Napolitano Antonio; Martinelli Diego; Deodato Federica; Diodato Daria; Carrozzo Rosalba; Dionisi-Vici Carlo; Longo Daniela
Journal:  Neuroradiology       Date:  2020-07-22       Impact factor: 2.804

6.  A meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations.

Authors:  Xueli Chang; Yaxin Wu; Jie Zhou; Huaxing Meng; Wei Zhang; Junhong Guo
Journal:  Medicine (Baltimore)       Date:  2020-01       Impact factor: 1.889

7.  An interesting case of Leigh-like syndrome.

Authors:  K Bharani; G Gnanashanmugam; V Kamaraj; S Balasubramanian
Journal:  Ann Indian Acad Neurol       Date:  2012-10       Impact factor: 1.383

8.  A multicenter study on Leigh syndrome: disease course and predictors of survival.

Authors:  Kalliopi Sofou; Irenaeus F M De Coo; Pirjo Isohanni; Elsebet Ostergaard; Karin Naess; Linda De Meirleir; Charalampos Tzoulis; Johanna Uusimaa; Isabell B De Angst; Tuula Lönnqvist; Helena Pihko; Katariina Mankinen; Laurence A Bindoff; Már Tulinius; Niklas Darin
Journal:  Orphanet J Rare Dis       Date:  2014-04-15       Impact factor: 4.123

Review 9.  Involvement of the Spinal Cord in Mitochondrial Disorders.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  J Neurosci Rural Pract       Date:  2018 Apr-Jun

10.  LEIGH SYNDROME: A CASE REPORT WITH A MITOCHONDRIAL DNA MUTATION.

Authors:  Tânia Lopes; Margarida Coelho; Diana Bordalo; António Bandeira; Anabela Bandeira; Laura Vilarinho; Paula Fonseca; Sónia Carvalho; Cecília Martins; José Gonçalves Oliveira
Journal:  Rev Paul Pediatr       Date:  2018-10-29
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