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Results 1 - 10 of 36 for Intellectual developmental disorder with seizures language delay
  1. GRIN2A gene 
    ... that have features similar to epilepsy-aphasia spectrum disorders (described ... and developmental delay. Some people with mutations in chromosome 16 that ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  2. Valproic Acid and Pregnancy (Organization of Teratology Information Specialists)  
    Pregnancy and Medicines/Specifics ... Pregnancy and Medicines ... Organization of Teratology Information Specialists
    https://mothertobaby.org/fact-sheets/valproic-acid-pregnancy - External Health Links
  3. Chromosome 7 
    ... deletion syndrome. People with this form of the disorder have characteristic ... and language problems, and learning disabilities.People normally inherit one ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  4. 16p11.2 deletion syndrome 
    ... People with 16p11.2 deletion syndrome usually have developmental delay and ... and language. In 16p11.2 deletion syndrome, expressive language skills ( ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  5. Fragile X-Associated Disorders (FXD): A Handbook for Families, Health Care Providers, Counselors, and Educators (National Fragile X Foundation) - PDF  
    fragile x, handbook, 3rd edition, NFXF ... Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National Fragile X Foundation ... PDF
    https://fragilex.org/.../2012/01/Handbook-FXD_3rd_Edition.pdf - External Health Links
  6. Fragile X 101 (National Fragile X Foundation)  
    Fragile X Syndrome/Symptoms ... Fragile X Syndrome ... National Fragile X Foundation ... Fragile X Syndrome is caused by a full mutation of the FMR1 gene. Fragile X- ...
    https://fragilex.org/understanding-fragile-x/fragile-x-101 - External Health Links
  7. Fragile X syndrome 
    ... it. A family history of fragile X syndrome, developmental problems, or intellectual disability may not be present.
    https://medlineplus.gov/ency/article/001668.htm - Medical Encyclopedia
  8. 1q21.1 microduplication 
    ... Some people with a 1q21.1 microduplication have developmental delay and ... and language. Expressive language skills (vocabulary and the production of ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics
  9. Chromosome 17 
    ... gene causes lissencephaly. Lissencephaly is associated with severe intellectual ... Health Condition Potocki-Lupski syndrome ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  10. MBD5-associated neurodevelopmental disorder 
    MBD5-associated ... and the ability to understand speech, are very limited in affected individuals. By ...
    https://medlineplus.gov/...d5-associated-neurodevelopmental-disorder - Genetics
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