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Results 1 - 8 of 8 for FOXG1 disorder
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  1. ... FOXG1 syndrome has been known to have children. FOXG1-related disorder Genetic Testing Registry: Rett syndrome, congenital variant FOXG1 ... PubMed Florian C, Bahi-Buisson N, Bienvenu T. FOXG1-Related Disorders: From Clinical Description to Molecular Genetics. Mol Syndromol. ...
  2. ... PubMed Florian C, Bahi-Buisson N, Bienvenu T. FOXG1-Related Disorders: From Clinical Description to Molecular Genetics. Mol Syndromol. ...
  3. ... of Lennox-Gastaut syndrome in a patient with FOXG1-related disorder. Epilepsia. 2014 Nov;55(11):e116-9. doi: ...
  4. ... for CDKL5 Research International Foundation for Optic Nerve Disease International FOXG1 Syndrome Foundation International League Against Epilepsy International Pemphigus & ...
  5. ... from mutations in other genes. These conditions, including FOXG1 syndrome and CDKL5 deficiency disorder, were previously thought to be variant forms of ...
  6. ... long (q) arm of chromosome 14 can cause FOXG1 syndrome, which is a rare disorder characterized by impaired development and structural brain abnormalities. ...
  7. 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. ...
  8. 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 ... Most cases of Rett syndrome are caused by a change (also called a mutation) in a single gene. ... Eunice Kennedy Shriver ...