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Results 11 - 17 of 17 for Mandibular aplasia
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  1. Campomelic dysplasia From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic and Rare Diseases Information Center ... Find symptoms and other information about Campomelic dysplasia. ... Birth Defects/Specifics ... Birth Defects ... Bone Diseases/ ...
  2. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic and Rare Diseases Information Center ... Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ...
  3. ... M, Tremblay ML, Drouin J. Hindlimb patterning and mandible development require the Ptx1 gene. Development. 1999 May; ...
  4. ... the development of the ears and lower jaw (mandible). The identified mutations change single protein building blocks ( ... in this gene lead to the other developmental abnormalities associated with auriculo-condylar syndrome. More About This ...
  5. ... the development of the ears and lower jaw (mandible). The identified mutations change single protein building blocks ( ... in this gene lead to the other developmental abnormalities associated with auriculo-condylar syndrome. More About This ...
  6. Trigeminal Neuralgia From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Trigeminal Neuralgia/Learn More ... Trigeminal Neuralgia ... From the National Institutes of Health ... Trigeminal ...
  7. Treacher Collins Syndrome (Nemours Foundation)  
    ... and chin, hearing loss, vision loss, chin, craniofacial abnormalities, craniofacial, jawbone, mandibulofacial dysostocis ... some babies are born with. TCS causes distinctive abnormalities of the head and face, but doesn't ...
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