Displaying all 2 publications

Abstract:
Sort:
  1. Ismail F, Peyman M, Waran V, Vasudevan S, Subrayan V
    Optom Vis Sci, 2015 Apr;92(4 Suppl 1):S33-5.
    PMID: 25730333 DOI: 10.1097/OPX.0000000000000528
    To report a rare case of nasal chondroma presenting as hypertelorism.
    Matched MeSH terms: Hypertelorism/diagnosis*
  2. Chew FL, Visvaraja S
    J AAPOS, 2009 Aug;13(4):406-7.
    PMID: 19487143 DOI: 10.1016/j.jaapos.2009.02.007
    47 XYY syndrome is a sporadic condition in which the human male receives an extra Y chromosome. Few ocular associations have been documented. The authors report the first case of 47 XYY associated with morning glory syndrome, frontonasal meningoencephalocele, and midfacial defects.
    Matched MeSH terms: Hypertelorism/diagnosis
Related Terms
Filters
Contact Us

Please provide feedback to Administrator (afdal@afpm.org.my)

External Links