Distal arthrogryposis type 5

The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.

Distal arthrogryposis type 5 is an inherited developmental defect syndrome characterized by multiple congenital contractures of limbs, without primary neurologic and/or muscle disease that affects limb function, and ocular anomalies (ptosis, external ophtalmoplegia and/or strabismus). Intelligence is normal.

Visit the Orphanet disease page for more resources.

Last updated: 2/1/2012

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