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Results 1 - 10 of 15 for Holoprosencephaly sequence
  1. Nonsyndromic holoprosencephaly 
    Nonsyndromic holoprosencephaly is an abnormality of brain development that also affects the head and face. Normally, the brain divides into two halves (hemispheres) ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. Learning about Holoprosencephaly (HPE) From the National Institutes of Health (National Human Genome Research Institute)  
    Holoprosencephaly is a disorder caused by the failure of the the embryonic forebrain to sufficiently divide into ...
    https://www.genome.gov/Genetic-Disorders/Holoprosencephaly - External Health Links
  3. Hartsfield syndrome 
    Hartsfield syndrome is a rare condition characterized by holoprosencephaly, which is an abnormality of brain development, and ... 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
  4. 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 ... Hydrocephalus/Specifics ... Hydrocephalus ... Neural Tube Defects/Specifics ... Neural Tube Defects ... Brain Malformations/Specifics
    https://www.ninds.nih.gov/.../birth-disorders-brain-and-spinal-cord - External Health Links
  5. ZIC2 gene 
    ... ZIC2 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... are the second most common cause of nonsyndromic holoprosencephaly. The facial features of individuals with ZIC2 gene ...
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  6. SHH gene 
    ... SHH gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... mutations are the most common cause of nonsyndromic holoprosencephaly. These mutations reduce or eliminate the activity of ...
    https://medlineplus.gov/genetics/gene/shh - Genetics
  7. TGIF1 gene 
    ... TGIF1 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... are the fourth most common cause of nonsyndromic holoprosencephaly. These mutations disrupt the protein's ability to ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  8. 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
  9. PTCH1 gene 
    ... PTCH1 gene have been found to cause nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ... cell patterning. The signs and symptoms of nonsyndromic holoprosencephaly are caused by abnormal development of the brain ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  10. 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
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