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  • Severe intellectual disability-poor language-strabismus . . .
    Symptoms of GAND include moderate to severe intellectual disability, poor speech development, and large head size Other signs and symptoms may include low muscle tone in children (childhood hypotonia), feeding problems, heart problems and shared facial features
  • What is GAND? - Helping Hands for GAND
    GAND stands for GATAD2B-associated neurodevelopmental disorder The GATAD2B gene is located on chromosome 1 (at 1q21 3) and is an important gene for normal cognitive development Most patients so far identified have had intellectual disability, low muscle tone, apraxia of speech, strabismus, macrocephaly, and distinct physical characteristics
  • GATAD2B-associated neurodevelopmental disorder (GAND . . .
    GAND’s clinical phenotype had substantial clinical overlap with other disorders associated with the NuRD complex that involve CHD3 and CHD4, with clinical features of hypotonia, intellectual disability, cardiac defects, childhood apraxia of speech, and macrocephaly
  • Gand Syndrome - MalaCards
    GAND syndrome is a neurodevelopmental disorder characterized by global developmental delay, motor delay, and moderate to severely impaired intellectual development Most patients have poor speech acquisition, hypotonia, and feeding difficulties in infancy
  • Resources — Gandaid
    what is gand? GAND stands for GATAD2B -associated neurodevelopmental disorder The GATAD2B gene is located on chromosome 1 (at 1q21 3) and is an important gene for normal cognitive development
  • GAND Syndrome - CAGS
    GAND syndrome is a neurodevelopmental syndrome characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development Most patients have poor speech acquisition, especially expressive language development, and may manifest signs of speech apraxia
  • Family support GAND - Rare Care World
    Supports individuals and families affected by GATAD2B-associated neurodevelopmental disorder (GAND), to increase awareness, and to work toward research and treatment opportunities to enrich the lives of those with this rare genetic condition





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