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Results 1 - 8 of 8 for FOXG1 syndrome
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  1. FOXG1 syndrome is a condition characterized by impaired development and structural brain abnormalities. Affected infants are small at ... amount of brain tissue known as white matter.FOXG1 syndrome affects most aspects of development, and children with ...
  2. ... and memory. Changes involving the FOXG1 gene cause FOXG1 syndrome, a rare disorder characterized by impaired development and ... important differences between the two conditions, so now FOXG1 syndrome is usually considered to be distinct from Rett ...
  3. ... long (q) arm of chromosome 14 can cause FOXG1 syndrome, which is a rare disorder characterized by impaired ... brain abnormalities and severe developmental problems characteristic of FOXG1 syndrome. It is unclear how the loss of additional ...
  4. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
  5. ... from mutations in other genes. These conditions, including FOXG1 syndrome and CDKL5 deficiency disorder, were previously thought to ...
  6. ... Research International Foundation for Optic Nerve Disease International FOXG1 Syndrome Foundation International League Against Epilepsy International Pemphigus & Pemphigoid ...
  7. 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
  8. ... S, Auvin S. A case of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder. Epilepsia. 2014 Nov;55(11):e116-9. doi: 10.1111/epi.12800. Epub 2014 Sep 29. Citation on PubMed Trevathan E. Infantile spasms and Lennox-Gastaut syndrome. J Child Neurol. 2002 Feb;17 Suppl 2: ...