Disorders


 

Spastic Paraplegia 4


Synonym(s): Hereditary Spastic Paraplegia, Spastin Type, HSP4, SPAST-Associated HSP, Spastic Paraplegia Type 4, SPG 4, SPG4

 

GeneReviewOMIM

GeneLocusProtein
SPAST2p24-p21Spastin

Laboratory Test Method Prenatal Carrier *
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA  
Burc Molecular Genetics Laboratory - Istanbul, Turkey  
CeGaT GmbH - Tuebingen, Germany  
Center for Human Genetics - University of Regensburg, Hehr Laboratory - Regensburg, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
diagenos - Osnabrueck, Germany  
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  
GGA - Galil Genetic Analysis - Kazerin, Israel  
GSTS Pathology, DNA Laboratory - London, Great Britain  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain  
InVitae Corporation - San Francisco, CA, USA  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Medgene, MedGene - Bratislava, Slovakia  
Medical Neurogenetics - Atlanta, GA, USA  
Praxis fuer Humangenetik Wien - Vienna, Austria  
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands  
Ruhr University, Human Genetics - Bochum, Germany  
Samsung Medical Center, Department of Laboratory Medicine and Genetics - Seoul, South Korea  
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea  
Sheffield Children's NHS Foundation Trust, Sheffield Diagnostic Genetics Service - Sheffield, Great Britain  
University Hospital of Tuebingen, Medical Genetics Tuebingen - Tuebingen, Germany  
University of Goettingen, Institute of Human Genetics - Goettingen, Germany  
University of Turku, Diagnostic DNA Laboratory - Turku, Finland  

* 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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