Baraitser-Rodeck-Garner syndrome: A very rare syndrome characterized primarily by mental retardation, premature fusion of skull bones, kidney anomalies, seizures and facial anomalies. More detailed information about the symptoms, causes, and treatments of Baraitser-Rodeck-Garner syndrome is available below.
See full list of 9 symptoms of Baraitser-Rodeck-Garner syndrome
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Baraitser-Rodeck-Garner syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Baraitser-Rodeck-Garner syndrome, or a subtype of Baraitser-Rodeck-Garner syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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