Synonyms: Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome
A rare genetic syndromic intellectual disability disorder characterized by craniofacial features global developmental delay intellectual disability and variable neurobehavioral abnormalities (autism spectrum disorder aggressiveness and self-injury). Additional features include vision abnormalities and variable sensorineural hearing loss as well as short stature hypotonia and gastrointestinal manifestations (e.g. poor feeding gastroesophageal reflux constipation).
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version June 2026
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White-Sutton syndrome?
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Advocacy Organizations
Cure Pogz Disorders Foundation
Our Mission is to urgently improve the lives of individuals and families affected by POGZ gene disorders by funding and accelerating cutting-edge science to discover treatments integral to our Path to Cure
PPP2CA Pathways
PPP2CA Pathways connects families, shares strength, and supports the research community in the search for answers to Houge-Janssens Syndrome type 3.
ReNU2 United
ReNU2 United fosters collaboration, supports families, raises awareness, and advances research into RNU2-2-related neurodevelopmental disease.
Uganda Alliance of Patients Organization
Supporting patients to access quality, safe and patient-centered healthcare services.
White Sutton Syndrome Foundation
The mission of the White Sutton Syndrome Foundation is to build a community that will improve the quality of life for those diagnosed with White Sutton Syndrome and their families, to educate others about this condition and to fund research in order to better understand its symptoms, treatments and prognosis.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.