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Results 1 - 9 of 9 for Holoprosencephaly 3
  1. Nonsyndromic holoprosencephaly 
    ... sequence Holoprosencephaly National Organization for Rare Disorders (NORD) HOLOPROSENCEPHALY 3; HPE3 HOLOPROSENCEPHALY 4; HPE4 HOLOPROSENCEPHALY 2; HPE2 HOLOPROSENCEPHALY ...
    https://medlineplus.gov/.../condition/nonsyndromic-holoprosencephaly - Genetics
  2. Learning about Holoprosencephaly (HPE) From the National Institutes of Health (National Human Genome Research Institute)  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Holoprosencephaly is a disorder caused by the failure of the the embryonic forebrain to ...
    https://www.genome.gov/Genetic-Disorders/Holoprosencephaly - External Health Links
  3. ZIC2 gene 
    ... ER, Stengel-Rutkowski S, Hennekam RC, Muenke M. Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired. Nat Genet. 1998 Oct;20(2):180-3. doi: 10.1038/2484. Citation on PubMed Dubourg ...
    https://medlineplus.gov/genetics/gene/zic2 - Genetics
  4. TGIF1 gene 
    ... two hemispheres. The signs and symptoms of nonsyndromic holoprosencephaly are caused by abnormal development of the brain and face. More About This Health Condition 5'-TG-3' interacting factor 5'-TG-3'-interacting factor 1 ...
    https://medlineplus.gov/genetics/gene/tgif1 - Genetics
  5. SIX3 gene 
    ... two hemispheres. The signs and symptoms of nonsyndromic holoprosencephaly are caused by abnormal development of the brain and face. More About This ... PubMed SIX HOMEOBOX ...
    https://medlineplus.gov/genetics/gene/six3 - Genetics
  6. Hartsfield syndrome 
    ... syndrome Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Holoprosencephaly, hypertelorism, and ectrodactyly syndrome ... Dhamija R, Babovic-Vuksanovic D. FGFR1-Related Hartsfield Syndrome. 2016 Mar 3 [updated 2022 May 12]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  7. PTCH1 gene 
    ... syndrome. Other signs and symptoms related to 9q22.3 microdeletions (such as delayed ... nonsyndromic holoprosencephaly. This condition occurs when the brain fails to ...
    https://medlineplus.gov/genetics/gene/ptch1 - Genetics
  8. 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
  9. Trisomy 13 
    ... structure of the brain. The problem is called holoprosencephaly. It is the joining together of the 2 ...
    https://medlineplus.gov/ency/article/001660.htm - Medical Encyclopedia