It is possible that the main title of the report Wieacker Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Apraxia, Oculomotor, with Congenital Contractures and Muscle Atrophy
- Contractures of Feet, Muscle Atrophy, and Oculomotor Apraxia
- Wieacker-Wolff Syndrome
Wieacker syndrome is a rare, slowly progressive, genetic disorder characterized by deformities of the joints of the feet (contracture), muscle degeneration (atrophy), mild mental retardation and an impaired ability to move certain muscles of the eyes, face and tongue. Wieacker syndrome is inherited as an X-linked recessive trait.
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NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases
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It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
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Last Updated: 1/5/2012
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