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Results 1 - 10 of 10 for Holoprosencephaly 2
  1. Nonsyndromic holoprosencephaly 
    ... Disorders (NORD) HOLOPROSENCEPHALY 3; HPE3 HOLOPROSENCEPHALY 4; HPE4 HOLOPROSENCEPHALY 2; HPE2 HOLOPROSENCEPHALY 1; HPE1 HOLOPROSENCEPHALY 6; HPE6 HOLOPROSENCEPHALY ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. TGIF1 gene 
    ... V. Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations. Hum Genet. 2003 Feb;112(2): ... Pasquier L, Henry C, Odent S, David V. Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2- ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  3. SIX3 gene 
    ... hedgehog expression in the ventral forebrain and causes holoprosencephaly. Dev Cell. 2008 Aug;15(2):236-47. doi: 10.1016/j.devcel.2008. ... the homeodomain of the human SIX3 gene cause holoprosencephaly. Nat Genet. 1999 Jun;22(2):196-8. doi: 10.1038/9718. Citation on ...
    https://medlineplus.gov/genetics/gene/six3 - Genetics
  4. ZIC2 gene 
    ... Pasquier L, Henry C, Odent S, David V. Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2- ... E, Muenke M. Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 ... Epub 2009 Dec 2. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  5. SHH gene 
    ... Pasquier L, Henry C, Odent S, David V. Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2-8. Citation on PubMed or Free article on PubMed Central Monuki ES. ... development and holoprosencephaly. J Neuropathol Exp Neurol. 2007 Jul;66(7): ...
    https://medlineplus.gov/genetics/gene/shh - Genetics
  6. PTCH1 gene 
    ... PTCH1 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to divide into two halves during early development. PTCH1 gene mutations are ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  7. Trisomy 13 
    ... structure of the brain. The problem is called holoprosencephaly. It is the joining together of the 2 sides of the brain. Chromosome studies show trisomy ...
    https://medlineplus.gov/ency/article/001660.htm - Medical Encyclopedia
  8. Hartsfield syndrome 
    ... development before birth, the brain normally divides into two halves, the right and left hemispheres. Holoprosencephaly occurs when the brain fails to divide properly. ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  9. FGFR1 gene 
    ... with Hartsfield syndrome, a rare condition characterized by holoprosencephaly, which is an abnormality of brain development, and a malformation of the hands and feet called ectrodactyly. Some of these mutations affect one of the two copies of the FGFR1 gene in each cell, ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  10. Birth Disorders of the Brain and Spinal Cord From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Craniofacial Abnormalities/Specifics ... Craniofacial ...
    https://www.ninds.nih.gov/.../birth-disorders-brain-and-spinal-cord - External Health Links