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Results 1 - 10 of 11 for Forebrain defects
  1. Learning about Holoprosencephaly (HPE) From the National Institutes of Health (National Human Genome Research Institute)  
    ... caused by the failure of the the embryonic forebrain to sufficiently divide into the double lobes of the cerebral hemispheres.
    https://www.genome.gov/Genetic-Disorders/Holoprosencephaly - External Health Links
  2. Birth Disorders of the Brain and Spinal Cord From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Brain Diseases/Specifics ... Brain Diseases ... Neural Tube Defects/Specifics ... Neural Tube Defects ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Brain Malformations/ ...
    https://www.ninds.nih.gov/.../birth-disorders-brain-and-spinal-cord - External Health Links
  3. ZIC2 gene 
    ... Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation. Hum Mol Genet. 2008 Oct 1;17(19):2986-96. doi: 10.1093/hmg/ddn197. Epub 2008 Jul 9. Citation on PubMed
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  4. Brain Facts: Glossary (Society for Neuroscience)  
    Brain Diseases/Reference Desk ... Brain Diseases ... Society for Neuroscience
    https://www.brainfacts.org/Glossary - External Health Links
  5. Nonsyndromic holoprosencephaly 
    ... PubMed Monuki ES. The morphogen signaling network in forebrain development and holoprosencephaly. J Neuropathol Exp Neurol. 2007 ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  6. HESX1 gene 
    ... structures at the front of the brain (the forebrain), including the nerves that carry visual information from ... gland, optic nerves, and other brain structures. These abnormalities of brain development lead to the characteristic features ...
    https://medlineplus.gov/genetics/gene/hesx1 - Genetics
  7. Anophthalmia/microphthalmia-esophageal atresia syndrome 
    ... SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development. J Clin ...
    https://medlineplus.gov/...icrophthalmia-esophageal-atresia-syndrome - Genetics
  8. SOX2 gene 
    ... SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development. J Clin ... MT. Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice ...
    https://medlineplus.gov/genetics/gene/sox2 - Genetics
  9. Anencephaly (Centers for Disease Control and Prevention)  
    Neural Tube Defects/Specifics ... Neural Tube Defects ... Anencephaly is a birth defect in which a baby is born without parts of the brain and skull. ... Centers for ...
    https://www.cdc.gov/birth-defects/about/anencephaly.html - External Health Links
  10. SYNGAP1 gene 
    ... mutants is caused by isolated damage within developing forebrain excitatory neurons. Neuron. 2014 Jun 18;82(6): ...
    https://medlineplus.gov/genetics/gene/syngap1 - Genetics
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