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Results 11 - 20 of 21 for Craniofacial cleft
  1. Isolated Pierre Robin sequence 
    ... DA, Visel A, Lyonnet S. Identification of novel craniofacial regulatory domains located far upstream of SOX9 and ...
    https://medlineplus.gov/.../condition/isolated-pierre-robin-sequence - Genetics
  2. Hartsfield syndrome 
    ... the brain, bones of the head and face (craniofacial bones), and bones in the hands and feet. ... split hand/foot syndrome Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Holoprosencephaly, hypertelorism, and ectrodactyly syndrome Genetic ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  3. Crouzon syndrome 
    ... cell is sufficient to cause the disorder. CFD1 Craniofacial dysarthrosis Craniofacial dysostosis Craniofacial dysostosis syndrome Craniofacial dysostosis ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics
  4. FGFR1 gene 
    ... brain, the bones in the head and face (craniofacial bones), the bones in the hands and feet, ... condition show abnormal bone growth that leads to craniofacial abnormalities, including the premature fusion of certain bones ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  5. Fryns syndrome 
    ... Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia. Pediatrics. ...
    https://medlineplus.gov/genetics/condition/fryns-syndrome - Genetics
  6. Treacher Collins syndrome 
    ... crest cell formation and proliferation deficiencies that cause craniofacial abnormalities. Proc Natl Acad Sci U S A. ... Collins syndrome: current evaluation, treatment, and future directions. Cleft Palate Craniofac J. 2000 Sep;37(5):434. ...
    https://medlineplus.gov/genetics/condition/treacher-collins-syndrome - Genetics
  7. SOX9 gene 
    ... DA, Visel A, Lyonnet S. Identification of novel craniofacial regulatory domains located far upstream of SOX9 and ...
    https://medlineplus.gov/genetics/gene/sox9 - Genetics
  8. Nager syndrome 
    ... Halonen K, Hukki J, Arte S, Hurmerinta K. Craniofacial structures and dental development in three patients with ...
    https://medlineplus.gov/genetics/condition/nager-syndrome - Genetics
  9. Moebius syndrome 
    ... 0000334892.45979.d5. Citation on PubMed Children's Craniofacial Association: A Guide to Understanding Moebius Syndrome Verzijl ...
    https://medlineplus.gov/genetics/condition/moebius-syndrome - Genetics
  10. Apert syndrome 
    ... Moore M. Apert Syndrome: Outcomes From the Australian Craniofacial Unit's Birth to Maturity Management Protocol. J ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
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