Disorders


 

Familial Partial Lipodystrophy Type 2


Synonym(s): Familial Partial Lipodystrophy, Dunnigan Type, FPLD2

 

OMIM

GeneLocusProtein
LMNA1q22Prelamin-A/C

Laboratory Test Method Prenatal Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands  
Addenbrooke's Hospital, Molecular Genetics Laboratory - Cambridge, Great Britain  
ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA  
Baylor College of Medicine, John Welsh Cardiovascular Diagnostic Laboratory - Houston, TX, USA  
CeGaT GmbH - Tuebingen, Germany  
CGC Genetics - Porto, Portugal  
Denver Genetic Laboratories, University of Colorado, DNA Diagnostic Laboratory - Aurora, CO, USA  
diagenos - Osnabrueck, Germany  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany  
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA  
GeneDx - Gaithersburg, MD, USA  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  
Health in Code S.L. - A Coruña, Spain  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Medgene, MedGene - Bratislava, Slovakia  
Praxis fuer Humangenetik Wien - Vienna, Austria  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Royal Devon and Exeter Hospital, Department of Molecular Genetics - Exeter, Great Britain• Sequence analysis of select exons
  
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik - Basel, Switzerland• Linkage analysis
  
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany  
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA  
University of Greifswald, Institute of Human Genetics - Greifswald, Germany  
University of Iowa Hospitals and Clinics, Department of Pathology - Iowa City, IA, USA  
University of Minnesota, University of Minnesota Physicians Outreach Laboratory - Minneapolis, MN, USA  

* 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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