Medicine Atlas

How Healing Is Practiced
Sign In
Text size
100%
Theme
Condition

Pseudoxanthoma elasticum

Diseases of the Skin and Subcutaneous Tissue

Pseudoxanthoma elasticum is a genetic disease that causes mineralization of elastic fibers in some tissues. It is a hereditary connective tissue disorder resulting from autosomal recessive mutations in the ABCC6 gene on chromosome 16, requiring two defective gene copies to develop the disease. It predominantly affects the skin through yellowish papular lesions, the eyes through retinal calcification and vision problems, and blood vessels through premature atherosclerosis and cardiovascular complications, arising from reduced pyrophosphate levels that normally inhibit mineralization in peripheral tissues.

Facts
Classification
Body System
Integumentary System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 1
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
First Described
1896 1
Sources
1. Pseudoxanthoma elasticum (Wikipedia)
  • Lead paragraph
    Pseudoxanthoma elasticum (PXE) is a genetic disease that causes mineralization of elastic fibers in some tissues.
  • Lead paragraph, cause
    The condition results from autosomal recessive mutations in the ABCC6 gene located on chromosome 16.
  • Wikipedia intro: Pseudoxanthoma elasticum: 'genetic disease...caused by autosomal recessive mutations'
  • History section
    The first description of PXE that distinguished it from other xanthoma conditions was by Dr Ferdinand-Jean Darrier in 1896.
View the Source
2. World Health Organization ICD-10: ICD-10 Version:2019 - Q80-Q89
World Health Organization ICD-10Category Q82.8
Quote, Category Q82.8
Q82.8 Other specified congenital malformations of skin
View the Source
Comments (0)
No comments yet. Be the first to share a thought.
Reader Challenges (0)
No disputes yet. Spotted an error or a better source? Open the first one.