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Results 1 - 10 of 14 for brachycephaly
  1. Baller-Gerold syndrome 
    Baller-Gerold syndrome is a rare condition characterized by the premature fusion of certain skull bones (craniosynostosis) and abnormalities of bones in the ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  2. FGFR2 gene 
    ... Bonaventure J. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  3. UNC80 deficiency 
    ... These features can include a wide, short skull (brachycephaly); a triangular face shape with a prominent forehead ( ...
    https://medlineplus.gov/genetics/condition/unc80-deficiency - Genetics
  4. Potocki-Shaffer syndrome 
    ... features, which can include a wide, short skull (brachycephaly); a prominent forehead; a narrow bridge of the ...
    https://medlineplus.gov/genetics/condition/potocki-shaffer-syndrome - Genetics
  5. Muenke syndrome 
    ... on the diagnosis and clinical management of syndromic craniosynostoses. Childs Nerv Syst. 2012 Sep;28(9):1447- ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  6. Andermann syndrome 
    ... spaced eyes (ocular hypertelorism); a wide, short skull (brachycephaly); a high arch of the hard palate at ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  7. KBG syndrome 
    ... distinctive facial features include a wide, short skull (brachycephaly), a triangular face shape, widely spaced eyes (hypertelorism), ...
    https://medlineplus.gov/genetics/condition/kbg-syndrome - Genetics
  8. White-Sutton syndrome 
    ... unusually small head (microcephaly); a wide, short skull (brachycephaly); wide-set eyes (hypertelorism); a flat or sunken ...
    https://medlineplus.gov/genetics/condition/white-sutton-syndrome - Genetics
  9. Spastic paraplegia type 49 
    ... small head size (microcephaly); a wide, short skull (brachycephaly); a short, broad neck; and facial features described ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-49 - Genetics
  10. Jackson-Weiss syndrome 
    ... Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Int J Pediatr ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
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