Van Maldergem Wetzburger Verloes syndrome

Common Name(s)

Van Maldergem Wetzburger Verloes syndrome

Van Maldergem syndrome is an autosomal recessive disorder characterized by intellectual disability, typical craniofacial features, auditory malformations resulting in hearing loss, and skeletal and limb malformations. Some patients have renal hypoplasia. Brain MRI typically shows periventricular nodular heterotopia (summary by {1:Cappello et al., 2013}). Genetic Heterogeneity of Van Maldergem Syndrome See also VMLDS2 ({615546}), caused by mutation in the FAT4 gene ({612411}) on chromosome 4q28.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Van Maldergem Wetzburger Verloes syndrome" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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