These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Frontonasal dysplasia associated with tetralogy of Fallot.
    Author: De Moor MM, Baruch R, Human DG.
    Journal: J Med Genet; 1987 Feb; 24(2):107-9. PubMed ID: 3560167.
    Abstract:
    Three children with frontonasal dysplasia associated with tetralogy of Fallot are reported. All cases had true hypertelorism and a median nasal groove with absence of the nasal tip. There was no mental deficiency. The facial anomaly is a sporadic, non-genetic interference of the normal development of the face. This is the first report of frontonasal dysplasia associated with a cardiac defect. Multifactorial inheritance of this syndrome is proposed.
    [Abstract] [Full Text] [Related] [New Search]