Disorders


 

Myotonic Dystrophy Type 2


Synonym(s): DM2, Dystrophica Myotonica 2, Proximal Myotonic Myopathy (PROMM)

 

GeneReviewOMIM

GeneLocusProtein
CNBP3q21Cellular nucleic acid-binding protein

Laboratory Test Method Prenatal Carrier *
Alberta Children's Hospital, Molecular Diagnostic Laboratory - Calgary, Canada• Targeted mutation analysis
  
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA• Targeted mutation analysis
  
Centogene AG, Rare Disease Company - Rostock, Germany• Targeted mutation analysis
  
CGC Genetics - Porto, Portugal• Targeted mutation analysis
  
Children's Hospital of Eastern Ontario, Molecular Genetics Diagnostic Laboratory - Ottawa, Canada• Targeted mutation analysis
  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany• Targeted mutation analysis
  
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Targeted mutation analysis
  
Institute of Medical Genetics, All Wales Molecular Genetics Laboratory - Cardiff, Great Britain• Targeted mutation analysis
  
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands• Targeted mutation analysis
  
Medgene, MedGene - Bratislava, Slovakia• Targeted mutation analysis
  
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany• Targeted mutation analysis
  
Praxis fuer Humangenetik Wien - Vienna, Austria• Targeted mutation analysis
  
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands• Targeted mutation analysis
  
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
  
Tor Vergata University of Roma, School of Medicine, Servizio di Genetica Medica - Rome, Italy• Targeted mutation analysis
  
University Hospital Brno, Center of Molecular Biology and Gene Therapy - Brno, Czech Republic• 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.

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