Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Mutations in ABCC6 cause pseudoxanthoma elasticum.

Authors: Bergen, AA  Plomp, AS  Schuurman, EJ  Terry, S  Breuning, M  Dauwerse, H  Swart, J  Kool, M  Van Soest, S  Baas, F  Ten Brink, JB  De Jong, PT 
Citation: Bergen AA, etal., Nat Genet 2000 Jun;25(2):228-31.
Pubmed: (View Article at PubMed) PMID:10835643
DOI: Full-text: DOI:10.1038/76109

Pseudoxanthoma elasticum (PXE) is a heritable disorder of the connective tissue. PXE patients frequently experience visual field loss and skin lesions, and occasionally cardiovascular complications. Histopathological findings reveal calcification of the elastic fibres and abnormalities of the collagen fibrils. Most PXE patients are sporadic, but autosomal recessive and dominant inheritance are also observed. We previously localized the PXE gene to chromosome 16p13.1 (refs 8,9) and constructed a physical map. Here we describe homozygosity mapping in five PXE families and the detection of deletions or mutations in ABCC6 (formerly MRP6) associated with all genetic forms of PXE in seven patients or families.


Disease Annotations
Objects Annotated

Additional Information

RGD Object Information
RGD ID: 737772
Created: 2004-02-26
Species: All species
Last Modified: 2004-02-26
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.