U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Mandibuloacral dysplasia progeroid syndrome

Summary

Mandibuloacral dysplasia progeroid syndrome (MDPS) is an autosomal recessive severe laminopathy-like disorder characterized by growth retardation, bone resorption, arterial calcification, renal glomerulosclerosis, and hypertension (Elouej et al., 2020). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: MDPS, metaxin-2, MTX2
    Summary: metaxin 2

Clinical features

Help

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.