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Early developmental delay in Leigh syndrome spectrum disorders is associated with poor clinical prognosis

  • Published:2022-04 Issue:4 Volume:135 Page:342-349
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Tinker Rory J.,Falk Marni J.,Goldstein Amy,George-Sankoh Ibrahim,Xiao Rui,Adang Laura,Ganetzky Rebecca

Funder

National Institutes of Health

NIGMS

NIDDK

Intellectual and Developmental Disabilities Research Center

United Mitochondrial Disease Foundation

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference31 articles.

1. Mitochondrial DNA-associated leigh syndrome and NARP;Thorburn,1993

2. Pediatric Leigh syndrome: neuroimaging features and genetic correlations;Alves;Ann. Neurol.,2020

3. Leigh syndrome: one disorder, more than 75 monogenic causes;Lake;Ann. Neurol.,2016

4. A guide to diagnosis and treatment of Leigh syndrome;Baertling;J. Neurol. Neurosurg. Psychiatry,2014

5. Subacute necrotizing encephalomyelopathy in an infant;Leigh;J. Neurol. Neurosurg. Psychiatry,1951

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