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Results 1 - 10 of 14 for Craniofacial cleft
  1. Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 
    ... Dang DX, Lewis RA, Bree AF, Bacino CA. Craniofacial and anthropometric phenotype in ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Hay-Wells syndrome) in a ...
    https://medlineplus.gov/...odermal-defects-cleft-lip-palate-syndrome - Genetics
  2. Frontonasal dysplasia 
    Frontonasal dysplasia is a condition that results from abnormal development of the head and face before birth. People with frontonasal dysplasia have at least two ...
    https://medlineplus.gov/genetics/condition/frontonasal-dysplasia - Genetics
  3. SATB2-associated syndrome 
    ... the structure of the brain.The most common craniofacial anomalies in people with SATB2-associated syndrome are a high arch or an opening in the roof of the mouth (high-arched or cleft palate), a small lower jaw (micrognathia), and dental ...
    https://medlineplus.gov/genetics/condition/satb2-associated-syndrome - Genetics
  4. Blepharocheilodontic syndrome 
    ... in the development of the head and face (craniofacial development), including the eyelids and teeth.While the ... shortage of these proteins disrupts normal development, especially craniofacial development, which is thought to underlie the features ...
    https://medlineplus.gov/.../condition/blepharocheilodontic-syndrome - Genetics
  5. 3MC syndrome 
    ... the condition. Carnevale syndrome Carnevale-Krajewska-Fischetto syndrome Craniofacial-ulnar-renal syndrome Craniosynostosis with lid anomalies Malpuech ...
    https://medlineplus.gov/genetics/condition/3mc-syndrome - Genetics
  6. Cerebro-facio-thoracic dysplasia 
    ... symptoms of the condition. Cerebrofaciothoracic dysplasia CFSMR CFTD Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Pascual- ...
    https://medlineplus.gov/.../cerebro-facio-thoracic-dysplasia - Genetics
  7. 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
  8. 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
  9. 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
  10. 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
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