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Pseudoxanthoma elasticum (inherited or acquired)

MONDO:0024308

An inherited disorder that causes calcium and other minerals to accumulate in the elastic fibers of the skin, eyes, and blood vessels, and less frequently in other areas such as the digestive tract.

Also known as: PXE, pseudoxanthoma elasticum

6 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive inherited pseudoxanthoma elasticum (6) Acquired pseudoxanthoma elasticum (0) Inherited pseudoxanthoma elasticum (0) Pseudoxanthoma elasticum, forme fruste (0)

Broader categories

Disease (680) Human disease (14) Disease by body system or component (0) Integumentary system disorder (0)
Trials to join now! 3 Not yet finished but already full! 1 Completed 2
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  • New hope for babies with rare calcification disease: first drug trial launches

    Disease control Ongoing

    This study tests a new drug called INZ-701 in up to 16 infants (up to 1 year old) with rare genetic conditions (ENPP1 or ABCC6 deficiency) that cause dangerous calcium buildup in arteries and other problems. The main goal is to check the drug's safety and how the body handles it,…

    Phase: PHASE1 • Sponsor: Inozyme Pharma • Aim: Disease control

    Last updated Aug 12, 2026 00:00 UTC

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