Disorders


 

Leber Hereditary Optic Neuropathy


Synonym(s): Hereditary Optic Neuroretinopathy, Leber's Disease, Leber's Optic Atrophy, Leber's Optic Neuropathy, LHON

 

GeneReviewOMIM

GeneLocusProtein
MT-ND6mitochondria 

Laboratory Test Method Prenatal Carrier *
Asper Biotech Ltd., Asper Biotech - Tartu, Estonia• Targeted mutation analysis
  
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA• Targeted mutation analysis
  
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA• Sequence analysis of the entire coding region
  
Burc Molecular Genetics Laboratory - Istanbul, Turkey• Targeted mutation analysis
  
Center for Human Genetics, Inc - Cambridge, MA, USA• Targeted mutation analysis
  
Centre for Cellular and Molecular Biology, Molecular Diagnostics Division - Hyderabad, India• Targeted mutation analysis
  
Centre Hospitalier Universitaire de Grenoble, Biochimie Genetique et Molculaire - Grenoble, France• Sequence analysis of the entire coding region
• Targeted mutation analysis
  
CGC Genetics - Porto, Portugal• Targeted mutation analysis
  
Charles University in Prague, First Faculty of Medicine - General University Hospital in Prague, Department of Pediatrics and Adolescent Medicine, Laboratory for Study of Mitochondrial Disorders - Prague, Czech Republic• Sequence analysis of the entire coding region
• Targeted mutation analysis
  
Children's Mercy Hospital and Clinics, Molecular Genetics Laboratory - Kansas City, MO, USA• Targeted mutation analysis
  
Children's University Hospital, Human Genetics - Berne, Switzerland• Targeted mutation analysis
  
Columbia University, Molecular Neurogenetics Laboratory - New York, NY, USA• Targeted mutation analysis
  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany• Sequence analysis of the entire coding region
• Targeted mutation analysis
  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany• Sequence analysis of the entire coding region
• Deletion/duplication analysis
  
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel• Sequence analysis of the entire coding region
• Targeted mutation analysis
  
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA• Targeted mutation analysis
  
GeneDx - Gaithersburg, MD, USA• Targeted mutation analysis
  
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Targeted mutation analysis
  
HUSLAB, Laboratory of Genetics - Helsinki, Finland• Targeted mutation analysis
  
Institute of Medical Genetics, All Wales Molecular Genetics Laboratory - Cardiff, Great Britain• Targeted mutation analysis
  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain• Targeted mutation analysis
  
Karolinska University Hospital, Centre for Inherited Metabolic Diseases - Stockholm, Sweden• Targeted mutation analysis
  
London Health Sciences Centre, Molecular Diagnostic Laboratory - London, Canada• Targeted mutation analysis
  
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands• Targeted mutation analysis
  
Medgene, MedGene - Bratislava, Slovakia• Targeted mutation analysis
 
Medical Neurogenetics - Atlanta, GA, USA• Targeted mutation analysis
 
MGZ München, Medizinisch Genetisches Zentrum Mnchen - München, Germany• Sequence analysis of the entire coding region
 
National University Hospital, Molecular Diagnosis Centre - Department of Laboratory Medicine - Singapore, Singapore• Targeted mutation analysis
 
New Jersey Medical School, Institute of Genomic Medicine - Newark, NJ, USA• Targeted mutation analysis
 
Ohio State University, Molecular Pathology Laboratory - Columbus, OH, USA• Targeted mutation analysis
 
Pro Genetic, Inc, University Children's Genetics Laboratory - Glendale, CA, USA• Targeted mutation analysis
 
Radboud University Medical Centre, Laboratory of Genetic, Endocrine, and Metabolic Diseases - Nijmegen, Netherlands• Targeted mutation analysis
 
Rush University Medical Center, Genetics Laboratory - Department of Pathology - Chicago, IL, USA• Targeted mutation analysis
 
Samsung Medical Center, Department of Laboratory Medicine and Genetics - Seoul, South Korea• Targeted mutation analysis
 
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea• Sequence analysis of the entire coding region
 
Sir Ganga Ram Hospital, Center of Medical Genetics - New Delhi, India• Targeted mutation analysis
 
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain• Targeted mutation analysis
 
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany• Targeted mutation analysis
 
Transgenomic, Transgenomic - Omaha - Omaha, NE, USA• Mutation scanning of the entire coding region
• Targeted mutation analysis
 
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik - Basel, Switzerland• Targeted mutation analysis
 
University of Alberta, Molecular Diagnostic Laboratory - Edmonton, Canada• Targeted mutation analysis
 
University of Iowa, John and Marcia Carver Nonprofit Genetic Testing Laboratory - Iowa City, IA, USA• Targeted mutation analysis
 
University of Turku, Diagnostic DNA Laboratory - Turku, Finland• Sequence analysis of the entire coding region
• Targeted mutation analysis
 

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

Loading...