Article
Heterogeneous presentation in Leigh syndrome
L. Vilarinho,
L. Vilarinho
Department of Clinical Biology, Instituto de Genética Médica, Porto, Portugal
Department of Neurology, College of Physicians & Surgeons, Columbia University, New York, NY, USA
Search for more papers by this author C. Maia,
C. Maia
Department of Pediatrics, Hospital S. Januário, Macau
Search for more papers by this author T. Coelho,
T. Coelho
Department of Neurology, Hospital Geral de S. António, Porto, Portugal
Search for more papers by this author P. Coutinho,
P. Coutinho
Department of Neurology, Hospital Geral de S. António, Porto, Portugal
Search for more papers by this author F. M. Santorelli,
F. M. Santorelli
Department of Neurology, College of Physicians & Surgeons, Columbia University, New York, NY, USA
Search for more papers by this author
L. Vilarinho,
L. Vilarinho
Department of Clinical Biology, Instituto de Genética Médica, Porto, Portugal
Department of Neurology, College of Physicians & Surgeons, Columbia University, New York, NY, USA
Search for more papers by this author C. Maia,
C. Maia
Department of Pediatrics, Hospital S. Januário, Macau
Search for more papers by this author T. Coelho,
T. Coelho
Department of Neurology, Hospital Geral de S. António, Porto, Portugal
Search for more papers by this author P. Coutinho,
P. Coutinho
Department of Neurology, Hospital Geral de S. António, Porto, Portugal
Search for more papers by this author F. M. Santorelli,
F. M. Santorelli
Department of Neurology, College of Physicians & Surgeons, Columbia University, New York, NY, USA
Search for more papers by this author
First published: 01 September 1997
No abstract is available for this article.
REFERENCES
- 1DiMauro S, De Vivo DC (1996) Genetic heterogeneity in Leigh syndrome. Ann Neurol, 40: 5–7.
- 2Leigh D (1951) Subacute necrotizing encephalomyelopathy in an infant. J Neurol Neurosurg Psychiatry, 14: 216–221.
- 3Santorelli FM, Barmada MA, Pons R et al (1996) Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletion. Neurology, 47: 1320–1323.
