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Results 1 - 8 of 8 for foxg1
  1. FOXG1 syndrome 
    FOXG1 syndrome is a condition characterized by impaired development and structural brain abnormalities. Affected infants are small ... amount of brain tissue known as white matter.FOXG1 syndrome affects most aspects of development, and children ...
    https://medlineplus.gov/genetics/condition/foxg1-syndrome - Genetics
  2. FOXG1 gene 
    The FOXG1 gene provides instructions for making a protein known as forkhead box G1. This protein is a transcription factor, which means it helps regulate ...
    https://medlineplus.gov/genetics/gene/foxg1 - Genetics
  3. Chromosome 14 
    ... long (q) arm of chromosome 14 can cause FOXG1 syndrome, which is a rare disorder characterized by ... of chromosome 14 that is deleted includes the FOXG1 gene as well as several neighboring genes. Depending ...
    https://medlineplus.gov/genetics/chromosome/14 - Genetics
  4. Lennox-Gastaut syndrome 
    ... genetic disorder, such as tuberous sclerosis complex. CHD2 FOXG1 SCN1A SCN8A STXBP1 Additional Information from NCBI Gene: ... of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder. Epilepsia. 2014 Nov;55(11):e116- ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  5. What Causes Rett Syndrome? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Rett Syndrome/Genetics ... Rett Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes of Health
    https://www.nichd.nih.gov/health/topics/rett/conditioninfo/causes - External Health Links
  6. Developmental Disabilities (National Library of Medicine)  
    What are developmental disabilities? Developmental disabilities are conditions that are usually present at birth. They can affect a child's growth and ...
    https://medlineplus.gov/developmentaldisabilities.html - Health Topics
  7. Patient support and advocacy groups 
    ... Research International Foundation for Optic Nerve Disease International FOXG1 Syndrome Foundation International League Against Epilepsy International Pemphigus & ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  8. Rett syndrome 
    ... from mutations in other genes. These conditions, including FOXG1 syndrome and CDKL5 deficiency disorder, were previously thought ...
    https://medlineplus.gov/genetics/condition/rett-syndrome - Genetics