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Results 1 - 4 of 4 for Holoprosencephaly 11
  1. Nonsyndromic holoprosencephaly 
    ... 25 to 50 percent of all cases of holoprosencephaly, which affects an estimated 1 in 10,000 newborns. Mutations in 11 genes have been found to cause nonsyndromic holoprosencephaly. ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. PTCH1 gene 
    ... cell carcinoma. Int J Dermatol. 2007 Nov;46(11):1113-7. doi: ... are associated with holoprosencephaly. Hum Genet. 2002 Apr;110(4):297-301. ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  3. SIX3 gene 
    ... SIX3 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... are the third most common cause of nonsyndromic holoprosencephaly. Although mutations in this gene can cause mild ...
    https://medlineplus.gov/genetics/gene/six3 - Genetics
  4. FGFR1 gene 
    ... with Hartsfield syndrome, a rare condition characterized by holoprosencephaly, which is an abnormality of brain development, and ... is unclear how these changes lead specifically to holoprosencephaly and ectrodactyly, the characteristic features of Hartsfield syndrome. ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics