GATAD2B-associated neurodevelopmental disorder | |
---|---|
Other names | GAND |
Specialty | Medical genetics |
Usual onset | Birth |
Duration | Life-long |
Causes | Mutation in the GATAD2B gene. |
Prevention | none |
Prognosis | Medium, nearing good |
Frequency | very rare, only 78 cases have been described in medical literature |
Deaths | - |
GATAD2B-associated neurodevelopmental disorder is a rare genetic neurodevelopmental disorder which is characterized by severe intellectual disabilities, speech delays, hypotonia and facial dysmorphia.[1]
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